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AEMPSVFOI
1560 Events
Recall Or Safety Alert for All Getinge Volista domes of Access, StandOP, Triop and Quicklock models manufactured until December 2016.
Recall Or Safety Alert for Aristos MX / VX AXIOM system (part number 05895003) with 3D-TOP ACSS mot. (reference 03070039)
Recall Or Safety Alert for EZ1 DSP Virus Kit (48), reference 62724.
Recall Or Safety Alert for Craniofacial repair implant QuickFlap Neuro
Recall Or Safety Alert for Elements Shutter Unit with Buchanan heat attackers and tip for pulp heat test
Recall Or Safety Alert for Philips IntelliVue MX40 monitor. Product code 865351
Recall Or Safety Alert for Fargo, references FRGMIN4.2F120MP and FRGMIN4.2F135
Recall Or Safety Alert for D-RAD SMART PACK plate 4 holes right, standard.
Recall Or Safety Alert for Containers of the Comprehensive Shoulder System Instrument. References 595608, 595260 and 595261.
Recall Or Safety Alert for Harmonic Ace® Laparoscopic scissors with 5 mm diameter + tissue adaptation technology (length 23 cm), c. HAR23 product and 5 mm diameter Harmonic Ace® Laparoscopic Scissors + tissue adaptation technology (length 36 cm), c. HAR36 product
Recall Or Safety Alert for HeartwareTM HVADTM System
Recall Or Safety Alert for Tapered Screw-Vent® MTX tapered dental implant. Catalog number: TSVM4B10
Recall Or Safety Alert for GENESIS II 13MM TIBIAL PUNCH
Recall Or Safety Alert for Dräger Fabius anesthesia equipment.
Recall Or Safety Alert for Cardiosave Hybrid IABP
Recall Or Safety Alert for Eleganza de Luxe beds, model 1GL, manufactured during the period from 2003 to 2005.
Recall Or Safety Alert for Blood gas analyzers ABL9
Recall Or Safety Alert for ABL90 Flex analyzers.
Recall Or Safety Alert for ORTHO VISION and VISION analyzer Max for ORTHO BioVue cassettes
Recall Or Safety Alert for ThermoScientificTM OxoidTM OX1 Oxacillin, CT0159B.
Recall Or Safety Alert for CPAP respiratory systems
Recall Or Safety Alert for Mobile belt systems for stress tests (model: T2100)
Recall Or Safety Alert for Arthis Pheno Systems
Recall Or Safety Alert for Durex Condoms
Recall Or Safety Alert for RePlant® angled abutment, part no. 6050-52-60
Recall Or Safety Alert for Milling drill D1.5mm (Ref. 65050)
Recall Or Safety Alert for HexaPOD evo RT System
Recall Or Safety Alert for Prismaflex dialysis equipment.
Recall Or Safety Alert for PENTAX flexible duodenoscope, Models ED-3490TK and ED34-i10T
Recall Or Safety Alert for 3.5mm short insertion connector of the Phoenix tibial nail, reference 14-441045. Instrument kits containing the insertion connector: 14-400082, 14-400082S, 14-440065S, 14-442000-00, 14-442000S, 14-444000-00, 979105, 14-441045-00, 14-444000S
Recall Or Safety Alert for Central Venous Catheter of Various Lumens of ARROW
Recall Or Safety Alert for Betamix non-stick barrier gel
Recall Or Safety Alert for Tourniquet for extremities SAM XT-M, SAM XT-C and SAM XT-B.
Recall Or Safety Alert for Carina fan
Recall Or Safety Alert for Articulated loading units Covidien Endo GIA ™.
Recall Or Safety Alert for Urine test strips Combur10 Test UX, reference 11544373191 used with the Urine Analyzer URISYS 1100, reference 03617548001, all the batches prior to No. 29896101
Recall Or Safety Alert for Probe for Fluorescent In Situ Hybridization (FISH), cMYC (MYC) Breakapart, references: LPH010, LPH010-20, LPH010-S
Recall Or Safety Alert for PHYT slides from VITRO Chemistry Products, Product code 8298671
Recall Or Safety Alert for Channel connection material for endoscopic washer disinfectors Wassenburg
Recall Or Safety Alert for MONACO.
Recall Or Safety Alert for Infusion stopcock
Recall Or Safety Alert for Syringes, aspirators and kits for arterial blood gas samples (ABG) AirLife ™
Recall Or Safety Alert for Imola RX Analyzer, Catalog number RX 4900, GTIN 05055273206104
Recall Or Safety Alert for Accu-Chek Aviva and Accu-Chek Performa test strips
Recall Or Safety Alert for AMPLYA monitor, ref. IBAXXX700 and / or CPFCA (Coupled Plasma Filtration Adsorption) kit, ref. IB0600000.
Recall Or Safety Alert for Thermo Scientific ™ Remel ™ Agglutinating Sera R30161201-Salmonella H (gm), 30161301-Salmonella H (gp) and 30161401-Salmonella H (gq)
Recall Or Safety Alert for Artis zee / Q / Q.zen systems with Large Display DSC 5608-DC screen.
Recall Or Safety Alert for MagNA Pure System 24
Recall Or Safety Alert for Blue and green refills of the Stapler 45 of the da Vinci Xi® Surgical System
Recall Or Safety Alert for 3-way key, reference RO301M.
Recall Or Safety Alert for Alere Afinion ™ ACR control kit, catalog number 1116046
Recall Or Safety Alert for Line sets for Novaline brand hemodialysis: BL 24 (product code: 955307), BL 106 (product code: 955443), BL 200HDF (product code: 955444), BL 208 (product code: 955445), BL 211 SN (product code 955447)
Recall Or Safety Alert for Elecsys Vitamin D total II assay, reference 07464215190 used in MODULAR ANALYTICS E170, cobas e 411, cobas e 601 and cobas e 602. Elecsys Vitamin D total II assay, reference 07028148190, used in cobas e 801 analyzers.
Recall Or Safety Alert for Infusion peristaltic pump Volumed μVP7000
Recall Or Safety Alert for Bilirubinometer JM-103 and JM-105.
Recall Or Safety Alert for Dental autoclave model "GD-18L-D"
Recall Or Safety Alert for Sistema Atellica COAG 360, SMN 10707173 and 10759658
Recall Or Safety Alert for Sistema Atellica COAG 360, SMN 10707173 and 10759658
Recall Or Safety Alert for Somatom Go.Up (Ref. 11061628), Somatom Go.Now (Ref.11061618)
Recall Or Safety Alert for AbViser ™ Autovalve ™ intra-abdominal pressure monitoring (PIA) system, codes ABV601, ABV300 and ABV301
Recall Or Safety Alert for Intraclude ™ intra-aortic occlusion device, Model ICF100
Recall Or Safety Alert for Set of 0º stem and collar with fixing screws for Orthopedic Salvage System (OSS) modular arthrodesis, reference CP2606600
Recall Or Safety Alert for ASKINA GEL and ASKINA CALGITROL PASTE Codes: 001419SES, 001419SESCP and 6241505
Recall Or Safety Alert for BD Vacutainer® EDTA blood collection tubes and blood collection tubes BD Vacutainer® lithium heparin.
Recall Or Safety Alert for ENDOPATH® XCEL ™ 5mm trocar with Optiview technology, codes 2B5ST, 2B5LT, 2B5XT, 2CB5ST and 2CB5LT
Recall Or Safety Alert for Enteral nutrition probes with AL ballast, reference AL208G.
Recall Or Safety Alert for CalApp® software, component of the BÜHLMANN IBDoc® test for Calprotectin, version sw 1.5.06 (iOS) / 1.5.07 (Android) and previous
Recall Or Safety Alert for Magnetic Resonance Systems: T5, T10-NT, ACSNT, Intera 0.5T / 1.0T / 1.5T, Achieva 1.5T, Multiva 1.5T, Ingenia CX 1.5T, Panorama 1.0T
Recall Or Safety Alert for Reagents of the ID-System system
Recall Or Safety Alert for LIFECODES HLA-B SSO Typing Kit, reference 628915 LIFECODES HLA-B eRES SSO Typing Kit, order number 628917
Recall Or Safety Alert for LIFE 18 - Theraline pro, reference 330-000-651
Recall Or Safety Alert for Set of staplers for prolapse and hemorrhoids procedures EEATM with DST SeriesTM technology.
Recall Or Safety Alert for Cardiovit AT-102 Plus Electrocardiograph and Spirometry Unit
Recall Or Safety Alert for Dimension GENT (DF12, 10444927) and Dimension Vista GENT (KD693, 10469971).
Recall Or Safety Alert for Soft-Trans embryo transfer catheter.
Recall Or Safety Alert for Automated hematology analyzer MEK-9100 Celltac G.
Recall Or Safety Alert for 708032: MultiDiagnost Eleva - 708033: UroDiagnost Eleva - 708034: MultiDiagnost Eleva with Flat Detector - 708035: MultiDiagnost Eleva with Flat Detector - 708036: MultiDiagnost Eleva - 708037: MultiDiagnost Eleva with Flat Detector - 708038: MultiDiagnos
Recall Or Safety Alert for "Cardiac Resynchronization Therapy Devices (CRT-D) and Implantable Automatic Defibrillators (ICDs) Model Family: Fortify ™, Fortify Assura ™, Quadra Assura ™, Quadra Assura MP ™, Unify ™, Unify Assura ™, Unify Quadra ™ , Promote Quadra ™, Ellips
Recall Or Safety Alert for Discovery Systems IGS 730/740 and Innova IGS 620/630/520/530/540.
Recall Or Safety Alert for SALSA MLPA probemix P060 SMA
Recall Or Safety Alert for Magik Thread (polydioxanone absorbable suture threads) indicated for face and body lifting.
Recall Or Safety Alert for Flex Arm Instrument (Model: 03.612.010)
Recall Or Safety Alert for Allura Xper with large screen monitor FlexVision
Recall Or Safety Alert for Needles guides ZNN and MDN.
Recall Or Safety Alert for RayStation 6 (RayPlan 2) and RayStation 7 (RayPlan 7)
Recall Or Safety Alert for FilmArray Blood Culture Identification (BCID) Panel with blood culture bottles BD BACTECTM. See BD BACTECTM catalog numbers affected in the company's notice.
Recall Or Safety Alert for Infusion pump Rythmic Evolution
Recall Or Safety Alert for Left Ventricular Assist System (LVAS) HeartMate 3 ™. Model number: 106524INT LVAS Kit HM 3.
Recall Or Safety Alert for Bone radiodensitometers DPX-NT, DPX Bravo, DPX Duo, DPX-MD, Prodigy and Prodigy Advance with enCORE software, versions 9.0 to 10.0.
Recall Or Safety Alert for MindFrame CaptureTM LP, models 300010, 300011, 300012 and 300013
Recall Or Safety Alert for Halyard closed suction kits with Flex connector: Halyard closed suction system for adults, double swivel elbow, Halyard turbo cleaning suction system for adults, double swivel elbow, Closed suction system with multi-port
Recall Or Safety Alert for Set of single-use flexible tubes for transanal endoscopic microsurgery (TEM). Model number: 4170.801.
Recall Or Safety Alert for Entroy pool lift. Model GAB1000-01-EU.
Recall Or Safety Alert for Accessory bag access device Alaris with SmartSite (Model: 10013365-0006)
Recall Or Safety Alert for Automatic External Defibrillators (AEDs): • HeartStart FRx, models 861304 and 861305, • HeartStart (HS1) Home and HeartStart (HS1) OnSite; M5066A, M5067A, M5068A models manufactured between September 2002 and February 2013.
Recall Or Safety Alert for Chest catheter and Portex connection tube
Recall Or Safety Alert for Infiniti Plus single-angle, non-sterile bracket (adapter) for use with 18L15 ultrasound scanner BK 8870, reference 620-116
Recall Or Safety Alert for RegJoint
Recall Or Safety Alert for Ultrasound imaging systems: LOGIQ 9 and lOGIQ E9; Vivid 7, Vivid E7, Vivid 9, Vivid E9, Vivid E80, Vivid E90, Vivid E95
Recall Or Safety Alert for Monoclonal Mouse Anti-Pneumocystis Jiroveci, Clone 3F6. Monoclonal Mouse Anti-Human Leukaemia, Hairy Cell, Clone DBA.44
Recall Or Safety Alert for Intraocular lenses Synthesis.
Recall Or Safety Alert for Ureic Nitrogen Reagent Kit (UN), reference 10309051, used in ADVIA® Chemical Systems 1800, 2400 and XPT.
Recall Or Safety Alert for Plasma filters MICROPLAS
Recall Or Safety Alert for Analyzer Alere AfinionTM 2, catalog number 1116553, 1116556 and 1116557
Recall Or Safety Alert for TEE probes models 6VT-D, 6Tc, 6Tc-RS, 6T, 6T-RS, 9T and 9T-RS.
Recall Or Safety Alert for BD Vacutainer Plus blood collection tubes with citrate, catalog number 363048
Recall Or Safety Alert for InterActiveTM healing screw, catalog no. 6530-15, batch 98151
Recall Or Safety Alert for Ambulance stretcher attachment, Power-Load, Model 6390. Units manufactured between January 1 and December 31, 2016
Recall Or Safety Alert for EliA Intrinsic Factor well, reference 14-5668-01
Recall Or Safety Alert for Modular analytical platform cobas® 8000, cobas e 801 module (GMMI 07682913001)
Recall Or Safety Alert for Fischer Cone Biopsy Excisor®, reference 900-151
Recall Or Safety Alert for Sample collection device PerkinElmer 226, Model 415416, 1600039101-106, 1600039127, 1600044601-636 and 1600045252
Recall Or Safety Alert for IH-1000, catalog number 001000.
Recall Or Safety Alert for Centricity PACS-IW.
Recall Or Safety Alert for BeGraft Peripheral Stent Graft System (BGP), references BGP5709_1 and BGP5709_2
Recall Or Safety Alert for Lipase test in RX Series systems
Recall Or Safety Alert for StoneBreaker® Pneumatic Lithotripter and Accessories (StoneBreaker® Exhaust Pipe Connector, StoneBreaker® Exhaust Pipe, StoneBreaker® Probe Connector, StoneBreaker® Sterilization Connector, StoneBreaker® CO2 Cartridge, Single Probe)
Recall Or Safety Alert for Servo ventilation systems
Recall Or Safety Alert for Modules TCM4 combi, TCM CombiM and TCM Tosca
Recall Or Safety Alert for Diluents of CTNI, MULTI 1 and MULTI 2 samples for the Dimension Vista® System
Recall Or Safety Alert for Surgical table column OTESUS 116001C0, serial number from 1 to 552, and OTESUS 116001D0, serial number from 1 to 34.
Recall Or Safety Alert for TROCAR CATH 40CM 20FR X 10, art 8888561043, lot 1724119864; YANKAUER FINE X50, item 8888504001, lot 1722020264, YANKAUER HIGH, item 8888502005, item 1726918664; YANKAUER REG W / TT, item 8888501023, item 1712221264; YANKAUER REG X50, article 8888501007, item 1726220064
Recall Or Safety Alert for Somatom Go.Up and Somatom Go.Now
Recall Or Safety Alert for Da Vinci X surgical system, model X 4200
Recall Or Safety Alert for Fabian Therapy Evolution Respirator, Reference 12001
Recall Or Safety Alert for On-X® bivalve mechanical valve prostheses, see product codes in the Notice of Company Notice
Recall Or Safety Alert for Blood collection flap "BD Vacutainer Push Button Blood Collection Set", Catalog Number: 367342
Recall Or Safety Alert for Infinity® Patient Monitor M540, Infinity Acute Care System (IACS) physiological monitoring system
Recall Or Safety Alert for Kit Beta-2-microglobulin in urine, codes LK043.L.OPT and LK043.L.OPT.A, for use with the Optilite analyzer.
Recall Or Safety Alert for 12 Cardio M and Cardio M PLUS Electrocardiographs
Recall Or Safety Alert for Cook Vacuum Pump TM vacuum pump. Reference number KMAR-5200.
Recall Or Safety Alert for VISURE Flu A, Flu B & RSV Real Time PCR Detection Kit in BD MAXTM Systems. Reference 444200.
Recall Or Safety Alert for VIDAS FSH, reference 30407
Recall Or Safety Alert for Thermo Scientific ™ Remel ™ R30166601 - Neisseria meningitidis Poly AD and Thermo Scientific ™ Remel ™ R30167001 - Neisseria meningitidis Group D
Recall Or Safety Alert for VeriQ, VeriQ C and Mira Q systems
Recall Or Safety Alert for FO SP laryngoscope handle, Article no. F-001.22.815
Recall Or Safety Alert for Zenith® Branch Iliac Vascular Endoprosthesis (ZBIS).
Recall Or Safety Alert for Implantable cardiac defibrillators (ICDs) and defibrillators with cardiac resynchronization therapy (CRT-Ds) Platinium, models DF4: VR 1240, DR 1540, CRT-D 1741, SonR CRT-D1841, 4LV CRT-D 1744, 4LV SonR CRT-D 1844
Recall Or Safety Alert for Urine microscopy analyzer of the iQ200 Series (all reference number)
Recall Or Safety Alert for 17 ° Multi-Unit Abutment Conical Connection NP 2.5mm. Model 36614.
Recall Or Safety Alert for Reverse osmosis units, various models manufactured between 2000 and 2017
Recall Or Safety Alert for Flow cytometry system AQUIOS CL, catalog number B30166, All software versions (2.0, 2.0.1 and 2.1)
Recall Or Safety Alert for Patient warming system Geratherm UniqueTemp
Recall Or Safety Alert for MindFrame CaptureTM LP
Recall Or Safety Alert for Patient tables of the CAT Systems: Ingenuity Flex, Ingenuity CT, Ingenuity Core, Ingenuity Core128, Brilliance iCT and Brilliance Big Bore.
Recall Or Safety Alert for Thermo Scientific ™ Oxoid ™ Cetrimide Agar culture medium (EP, USP, JP, BP), PO1168A
Recall Or Safety Alert for Versatex ™ monofilament mesh, 50 x 50 cm, Article code VTX5050M
Recall Or Safety Alert for Catheter repair kits, reference RPK-01, distributed between August 2016 and February 2018.
Recall Or Safety Alert for Kit Lives LH, reference 30406
Recall Or Safety Alert for 24-hole cannula, reference LP0305-05; Continuous injection cannula, ref LP0601-01; Continuous injection cannula, reference LP0601-05; Lipo'Art Premium Kit, reference LP1101-01; Injection Cannula Punta Oliva, reference LP0501-10
Recall Or Safety Alert for CUNA PEDIATRICA.MODELO NANO
Recall Or Safety Alert for Spacer blocks of the "Persona" knee partial denture, sizes 8,9,10,12 and 14 mm
Recall Or Safety Alert for Artisan Classic (AR100), Artisan Link (AR210) and Artisan Link Pro (AR310).
Recall Or Safety Alert for Linear Digital Accelerators (LINAC) of the PRIMUS ™ and ONCOR ™ type
Recall Or Safety Alert for Ultrafilter U9000, reference 112062.
Recall Or Safety Alert for VITEK® 2 Compact 15/30 systems
Recall Or Safety Alert for SOMATOM Emotion SOMATOM Spirit SOMATOM Scope / Power, SOMATOM Perspective SOMATOM Sensation
Recall Or Safety Alert for SOMATOM Emotion (2007) SOMATOM Spirit / Power SOMATOM Scope / Power, SOMATOM Perspective SOMATOM Sensation, SOMATOM Huan Yue
Recall Or Safety Alert for Pericardiocentesis kit catalog number PC101EU and PC803EU
Recall Or Safety Alert for Intrauterine devices (IUD), models: ANCORA, NOVAPLUS®, GOLD T®
Recall Or Safety Alert for RFA BarrierTM 360 Express balloon catheter
Recall Or Safety Alert for Infinity Acute Care System physiological monitoring system (IACS) Infinity® M540 patient monitor
Recall Or Safety Alert for Injection pipette model number / catalog LICR-OD5.
Recall Or Safety Alert for Agilia Volumat infusion lines, manufactured between August 2017 and March 2018.
Recall Or Safety Alert for ETEST PO1024 (Polymyxin B), reference 533400.
Recall Or Safety Alert for Capio ™ suture capture devices (SLIM, Standard, Open Access, RP); Uphold ™ LITE vaginal support support with Capio ™ SLIM; Pinnacle ™ anterior pelvic floor repair kit; Pinnacle ™ LITE REAR pelvic floor repair kit with Capio SLIM
Recall Or Safety Alert for Heating systems for patients, models W-150T, W-300 and W-500D, manufactured until December 2012; Blankets / heating mattresses, various models, manufactured since February 2013.
Recall Or Safety Alert for Progressa ™ P7500 Bed Systems
Recall Or Safety Alert for Oxoid ™ Culture Medium Mueller-Hinton Broth Code CM0405B
Recall Or Safety Alert for BD OneFlow B-CLPD T1 Catalog No. 659293
Recall Or Safety Alert for Vylife, reference 7506.02; Vylife kit, references 5582.700 and 5582.802
Recall Or Safety Alert for LabPro data management system, catalog us 6000-0076, 6000-0078 and 6000-0035
Recall Or Safety Alert for LabPro data management system, catalog us 6000-0076, 6000-0078 and 6000-0035
Recall Or Safety Alert for VP-7000 video processor used in endoscopes of the 700 series
Recall Or Safety Alert for EliA anti-TSH-R well, reference 14-5639-01
Recall Or Safety Alert for MeniCare Soft 70ml, catalog number MAN100561
Recall Or Safety Alert for LIFECODES HLA-A SSO and LIFECODES HLA-A eRES SSO typing kits used with the MATCH-IT software! DNA
Recall Or Safety Alert for Motiva ® breast implants
Recall Or Safety Alert for DuowireTM Bi-Flex guide, reference AEBD35.
Recall Or Safety Alert for INGEVITY MRI stretch / retractable stimulation cable (active fixation).
Recall Or Safety Alert for INGEVITY MRI stretch / retractable stimulation cable (active fixation).
Recall Or Safety Alert for Volumed ALP0J1F, Lot No. 17PH051 and 17PH051.1
Recall Or Safety Alert for Thermo Scientific ™ Remel ™ Vibrio Cholerae Inaba Agglutination Serum, Reference: R30165101.
Recall Or Safety Alert for Advanced Revolve® adipose system
Recall Or Safety Alert for Nellix® EndoVascular Aneurysm Sealing System
Recall Or Safety Alert for Elevators for pools Oxford Dipper, models OP10013 and OP10014.
Recall Or Safety Alert for Cisco ASA 5506-X Network Firewall, model 867098.
Recall Or Safety Alert for Syringe pumps AlarisTM GS, GH, CC, TIVA, PK (codes with prefix 8001, 8002, 8003, 8004, 8005), manufactured before September 2008 and Syringe pumps AsenaTM GS, GH, CC, TIVA, PK (codes with prefix 8001, 8002, 8003, 8004 and 8005
Recall Or Safety Alert for CP5 centrifugal pumps used in combination with Livanova heart-lung machines (HLM), manufactured before February 10, 2017.
Recall Or Safety Alert for Electric wheelchairs Permobil C300, C350, C400 and C500 with seats Corpus II, Corpus II LR and Corpus KB, distributed between June 2011 and February 2017
Recall Or Safety Alert for Surgical lamps Hanaulux 2000, Hanaulux 3000 and XTEN series, with domes 5017 MAQUET HLX 2004-5 DF, HLX 3004-5 DF, XTEN DF when used with the spring arms ONDAL Acrobat 2000, manufactured between January 2004 and December 2006.
Recall Or Safety Alert for Certain tests used in the Dimension and Dimension Vista Systems.
Recall Or Safety Alert for Hexagonal retention screwdriver 2.5 mm with GemLock® (RHD2.5)
Recall Or Safety Alert for Bard®Max-Core® Disposable Biopsy Instrument. See references and affected lot numbers in Annex 1 of the company's notice
Recall Or Safety Alert for Vanguard CR Tibial Insert and Vanguard CR Tibial Tibial Insert
Recall Or Safety Alert for Centrifugal and eccentric modular epiphysis implants from the DELTA XTEND® Reverse Shoulder System
Recall Or Safety Alert for Magic3® intermittent catheter, with sure-gripTM silicone sleeve with hydrophilic coating (lengths of 40cm and 25cm).
Recall Or Safety Alert for CareLinkTM iPro therapy management software (MMT-7340).
Recall Or Safety Alert for Auriga 30 and Auriga XL 4007 laser system.
Recall Or Safety Alert for Deflectable FlexCath Advance ™ Introducer - Model Number 4FC12
Recall Or Safety Alert for Dual-lumen catheters ECLIPSE2L and COPERNIC2L
Recall Or Safety Alert for SOMATOM Definition AS.
Recall Or Safety Alert for Neoplastine® CI Plus (2) (ref 00374), Neoplastine® CI Plus (5) (ref 00375), STA - Neoplastine ® CI (5) (ref 00605), STA - Neoplastine ® CI Plus (5) ( ref 00606).
Recall Or Safety Alert for FLEX TCM5 monitors -TCM5 BASIC.
Recall Or Safety Alert for FLEX TCM5 monitors -TCM5 BASIC.
Recall Or Safety Alert for GORE TAG Conformable thoracic endoprosthesis, model TGE 212110.
Recall Or Safety Alert for WECK® Auto Endo5® Automatic Hem-o-lok® clip applicators. Product code AE05ML.
Recall Or Safety Alert for Perfusion tube systems (PTS)
Recall Or Safety Alert for Tibial inserts GMK Sphere and PS Primary - All codes
Recall Or Safety Alert for FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor α, Clone EP1, Ready-to-Use (Dako Omnis), Catalog No .: GA084
Recall Or Safety Alert for ST Progesterone Assays AIA-PACK PROGII, Catalog No. 0025239 and ST AIA-PACK PROGII, Catalog No. 0025240
Recall Or Safety Alert for ABL800 analyzer with FLEXQ module, catalog number 393-800.
Recall Or Safety Alert for ABL800 analyzer with FLEXQ module, catalog number 393-800.
Recall Or Safety Alert for Distal shanks Tactys sizes S and M, catalog number: WIPTD11 and WIPTD13.
Recall Or Safety Alert for Flow cytometry system AQUIOS CL. Catalog No. B30166
Recall Or Safety Alert for Vital Signs Monitors from Philips SureSigns VSi and VS2 +
Recall Or Safety Alert for BC Thrombin Reagent Kits, OWNA11 Catalog Reference and Siemens Material Number 10446636
Recall Or Safety Alert for AIRO mobile TC. Model No. MobiCT-32
Recall Or Safety Alert for PROVEO 8 microscope, manufactured before July 2017
Recall Or Safety Alert for Catrix Collagen Healing Powder reference 5461014 and 5461000SOE
Recall Or Safety Alert for Hypo / hyperthermia systems TECOTHERM NEO equipped with a disposable temperature temperature probe model FMT 400 / AS-D with multi-purpose extension cable FMT400 / AEC-THT
Recall Or Safety Alert for Anaconda ™ ONE-LOK AAA endovascular graft system (bifurcated body), Anaconda ™ iliac endovascular graft system and Anaconda ™ AAA endovascular graft system.
Recall Or Safety Alert for Flow cytometry system AQUIOS CL, NP B30166
Recall Or Safety Alert for Flow cytometry system AQUIOS CL, NP B30166
Recall Or Safety Alert for Flow cytometry system AQUIOS CL, NP B30166
Recall Or Safety Alert for Artis systems with wireless footswitch.
Recall Or Safety Alert for HemosiL ReadiPlasTin (20mL), reference 00020301400.
Recall Or Safety Alert for Assay for in vitro diagnosis "XPERT EV of Cepheid", Ref. GXEV-100N-10.
Recall Or Safety Alert for Posterior stabilized femoral components of the Vanguard Knee System open drawer
Recall Or Safety Alert for Azurion cardiovascular intervention systems, models 722078 (Azurion 7 M12) and 722079 (Azurion 7 M20)
Recall Or Safety Alert for TAC Systems Philips Ingenuity CT, Ingenuity Core and Ingenuity Core128 and Brilliance 64, Software version 4.1.6
Recall Or Safety Alert for Philips Brilliance iCT TAC Systems, Software Version 4.1.6
Recall Or Safety Alert for Specific instruments of hip and traumatology: Drills, flexible shafts and intramedullary bur
Recall Or Safety Alert for Venous cannula FlexFlow ™, model 200-200
Recall Or Safety Alert for ABX PENTRA HbA1c WB Cal, reference A11A01703.
Recall Or Safety Alert for Insert expanSys metamys of acetabular cups expanSys, see references affected in the notice of the company
Recall Or Safety Alert for Delta cup impactor / positioner / aligner, model 9057.20.555.
Recall Or Safety Alert for Integral Knee System Optetrak® LogicTM
Recall Or Safety Alert for Neuray® Lentins and Neurosurgical Strips, Lentines and Merocel® Neurosurgical Buffers
Recall Or Safety Alert for ERGO
Recall Or Safety Alert for Emergency delivery kit, lots 94510101A and 96421801A, which contain lot 0816 of the device
Recall Or Safety Alert for Guided surgery kit Spectra System® / LegacyTM
Recall Or Safety Alert for Guided surgery kit Spectra System® / LegacyTM
Recall Or Safety Alert for THERMOCOOL SMARTTOUCH® SF unidirectional and bi-directional navigation catheter, THERMOCOOL SMARTTOUCH® unidirectional and bidirectional navigation catheter, THERMOCOOL SMARTTOUCH® SF NAV diagnostic / ablation catheter
Recall Or Safety Alert for Expansive lumbar interbody compartment LE-Cage
Recall Or Safety Alert for SERVO-air fans reference 66 82 000
Recall Or Safety Alert for Enzygnost HBsAg 6.0 Kit (10x96), catalog number OPFM05, material number Siemens 10446017, lot numbers 47023, 47119 and 47352 and Enzygnost HBsAg 6.0 Kit (2x96), catalog number OPFM03, material number Siemens 10446016, number batch
Recall Or Safety Alert for Ampoules S7745 AUTOCHECK 5+ LEVEL 2 Reference 944-075.
Recall Or Safety Alert for Radial Reload Endo GIA ™ black by Covidien with Tri-Staple ™ technology, reference EGIARADXT.
Recall Or Safety Alert for ATS 2200TS and ATS 4000TS pneumatic turnstiles distributed between January 2014 and June 2017.
Recall Or Safety Alert for Suture VICRYL RAPIDETM (Polyglactin 910)
Recall Or Safety Alert for Life-Point Automatic Defibrillators Pro AED models, bPLUS, mPLUS sold between October 11, 2013 and December 22, 2016 and Medeks brand defibrillation electrodes used with Life-P external defibrillators
Recall Or Safety Alert for Ziptight fixation for syndesmosis of the ankle, reference 904759
Recall Or Safety Alert for Zenit RA Scl-70 REF. 41418
Recall Or Safety Alert for Intensive care ventilators HAMILTON-C3 and HAMILTON-C2.
Recall Or Safety Alert for X-ray system Zexira DREX-ZX80 / E1
Recall Or Safety Alert for Anti-MCV - Kit Vimentina citrulinada Alegria, Reference ORG 248
Recall Or Safety Alert for Cystoscopy bridges and working inserts: Work insert, with one channel ramp, model number A20975A, Bridge, one channel, model number A20976A, Bridge, two channels, model number A20977A
Recall Or Safety Alert for MINICAP PROTEIN (E) 6, reference 2203
Recall Or Safety Alert for Quick set, Quick, Silhouette, Sure-T, Mio, Mio 30 infusion sets used with Medtronic's Minimed insulin infusion pumps
Recall Or Safety Alert for Quick set, Quick, Silhouette, Sure-T, Mio, Mio 30 infusion sets used with Medtronic's Minimed insulin infusion pumps
Recall Or Safety Alert for Defibrillation electrodes Skintact reference DF59N and Skintact reference DF59NC
Recall Or Safety Alert for Systems Artis zee and Artis Q.
Recall Or Safety Alert for External ventricular drainage set (EVD 30.001 .01) and external ventricular drainage set with plate and clamp (EVD 30.001.01).
Recall Or Safety Alert for Lentis foldable intraocular lenses, models that start with L-, LU-, or LS-
Recall Or Safety Alert for Thermo Fisher ScientificTM OxoidTM CAZ10 CEFTAZIDIME cartridges, reference CT1629B
Recall Or Safety Alert for Oral care products from Sage.
Recall Or Safety Alert for Implantable Impulse Generators NM (IPG) of the Infinity family and the Proclaim family
Recall Or Safety Alert for Affixus nails for hip fractures, distributed between May 2017 and July 2017
Recall Or Safety Alert for GXT NA extraction kit.
Recall Or Safety Alert for VOYANT electrosurgical generator, model EA010.
Recall Or Safety Alert for Quality controls Immunoassay Randox Acusera Premium and Premium Plus.
Recall Or Safety Alert for Strict Optical Trocar "5x55mm Kii Optical Z-Thread Dual Pack" Model CTR14
Recall Or Safety Alert for Medtronic DBS electrodes kits (deep brain stimulation), models 3387-XX, 3389-XX and 3391-XX.
Recall Or Safety Alert for BD MAXTM Vaginal Panel, reference 443710 BD MAX ™ CT / GC / TV, reference 442969 BD MAX ™ CT / GC, order number 442970
Recall Or Safety Alert for Thermo Scientific ™ Remel ™ Wellcolex ™ Color Shigella, Reference R30858401
Recall Or Safety Alert for Flow cytometry system AQUIOS CL, catalog number B30166
Recall Or Safety Alert for Fluorocell PLT reagent, reference CD-994-563 (Sysmex) and 06510299001 (Roche), used with the hematology analyzers of the XN Series of Sysmex
Recall Or Safety Alert for Drill guide of the locking compression plate (LCP) 1.5 f / Bit tip diameter 1.1 mm, reference 03.114.001.
Recall Or Safety Alert for Hydrophilic intraocular lens, Model: EC-3 of + 24.0D and + 10.0D.
Recall Or Safety Alert for Tests VERIS HCV, VERIS HBV, VERIS HIV-1 and VERIS CMV.
Recall Or Safety Alert for Accent ™ / Anthem ™, Accent MRI ™ / Accent ST ™, Assurity ™ / Allure ™ and Assurity MRI ™ pacemakers
Recall Or Safety Alert for BD Multitest ™ CD3 / CD8 / CD45 / CD4
Recall Or Safety Alert for Transjugular intrahepatic access equipment Ring, reference number: RTPS-100.
Recall Or Safety Alert for Disposable processing kits of the Cell Saver® 5/5 + system, reference 0291E-00
Recall Or Safety Alert for Extraction enzyme bottles, lots 1960420 and 1960621, included in the products: Streptex Rapid Latex Agglutination Test, reference R30950501 and Streptex Extraction Enzyme, reference R30951001.
Recall Or Safety Alert for ROSA 2.5.8.
Recall Or Safety Alert for Test Kit VITEK® 2 Gram-Positive Identification
Recall Or Safety Alert for Test Kit VITEK® 2 Gram-Positive Identification
Recall Or Safety Alert for EndoWrist® Stapler Release Kit (SRK) used with da Vinci Xi and da Vinci X Surgical Systems
Recall Or Safety Alert for EndoWrist® Stapler Release Kit (SRK) used with da Vinci Xi and da Vinci X Surgical Systems
Recall Or Safety Alert for Merlin @ Home ™ Remote Monitoring Transmitters Model EX2000
Recall Or Safety Alert for Novosyn Quick Undy 2/0 (3) 90CM HR37S, references C3046595 and G3046595
Recall Or Safety Alert for NIT-OCCLUD IMPLANTATION SHEATH
Recall Or Safety Alert for ATAR ™ extension cable for external pacemaker, model 53912; Reusable ATAR ™ extension cable, model 53912A, included with external pacemaker model 5391; Disposable ATAR ™ extension cord for external pacemaker, model 53912D.
Recall Or Safety Alert for VITEK® MS, reference 410895
Recall Or Safety Alert for Accu-Chek® Insight insulin infusion system.
Recall Or Safety Alert for FemoSeal ™ vascular closure system, Product Code C11202
Recall Or Safety Alert for Provisional and tibial measuring cups of the prosthesis Person
Recall Or Safety Alert for Transport circuits of 22mm Flextube with anti-rebreathing valve, references 2070000 and 2074000.
Recall Or Safety Alert for Percutaneous antenna of the Emprint TM ablation system with ThermosphereTM technology
Recall Or Safety Alert for ReNew ™ reusable tips (scissors, forceps and dissection)
Recall Or Safety Alert for Mammography systems FUJIFILM FDR-1000AWS, FDR-2000AWS, FDR-3000AWS and CR-IR363AWS
Recall Or Safety Alert for Mueller Hinton E Agar, from BioMérieux, references 413822, 413823 and 413825
Recall Or Safety Alert for Abbott RealTime HIV-1 trial, reference 02G31-010
Recall Or Safety Alert for 1. CORAIL® STEM WITH OFFSET FOR COXA VARA with collar size 9, Ref. 3L93709. 2. CORAIL® STEM WITH OFFSET without collar size 14, Ref. L20314.
Recall Or Safety Alert for Liquid Cardiac Control - Level 3, reference CQ5053, Randox.
Recall Or Safety Alert for Tracheostomy tube kit with UniPerc® adjustable rim, reference 100/897/080 CZ.
Recall Or Safety Alert for Quantrix BlueDiver, reference ANA25Q-24
Recall Or Safety Alert for central venous catheters
Recall Or Safety Alert for Tapestry Anti-Gravity model M320, manufactured before June 6, 2016.
Recall Or Safety Alert for Flexible cryotherapy probe for pulmonology ERBECRYO2 equipment
Recall Or Safety Alert for Oncentra® Brachy of the models of ring applicators or Venezia with microSelectron.
Recall Or Safety Alert for Catheters BEO NC PTCA
Recall Or Safety Alert for Temperature management system ARCTIC SUN 5000
Recall Or Safety Alert for ADVIA Centaur T3 kit (80 tests), reference 04779671 and ADVIA Centaur T3 kit (400 tests), reference 04779663, used in the ADVIA Centaur XPT systems.
Recall Or Safety Alert for ADVIA Centaur T3 kit (80 tests), reference 04779671 and ADVIA Centaur T3 kit (400 tests), reference 04779663, used in the ADVIA Centaur XPT systems.
Recall Or Safety Alert for HemosiL ReadiPlasTin (20mL), reference 00020301400
Recall Or Safety Alert for Agglutination serum Thermo Scientific ™ Remel ™ Vibrio Cholerae Ogawa, reference R30165201
Recall Or Safety Alert for Automated Peritoneal Dialysis Systems HomeChoice PRO, Reference R5C8320; HomeChoice Claria Automated Peritoneal Dialysis System, References 5C6M00 and 5C6M10
Recall Or Safety Alert for PLEGIOX Cardioplegia heat exchanger
Recall Or Safety Alert for Fans Monnal T50 Ref. KC027500, Monnal T50DE Ref. KC037600, Monnal T50JP Ref. KC037100
Recall Or Safety Alert for Fans Monnal T50 Ref. KC027500, Monnal T50DE Ref. KC037600, Monnal T50JP Ref. KC037100
Recall Or Safety Alert for Venous catheter / umbilical arterial code 270.03
Recall Or Safety Alert for Modular analyzer Cobas 8000
Recall Or Safety Alert for Modular analyzer Cobas 8000
Recall Or Safety Alert for ARTISET HD SN HC blood line, code 114533 and ARTISET HD DNL HC, code 955364.
Recall Or Safety Alert for Essure®
Recall Or Safety Alert for Fogarty catheter for adherent clots, models 140810 and 140806
Recall Or Safety Alert for Knee Femoral SC ESOP II
Recall Or Safety Alert for Sterile grease extraction system with Tissue-Trans Filtron filters 100, 500, 1000, 2000, MEGA 1500 and Syringe Fill 360
Recall Or Safety Alert for PERFLUORON® (Perfluoroctane)
Recall Or Safety Alert for Flexible Guide Catheter, models LLA300-F, LLA300-FB and LLA300N
Recall Or Safety Alert for BD MAXTM Vaginal Panel, reference 443710 BD MAX ™ UVE Specimen Collection Kit, order number 443376
Recall Or Safety Alert for "CAPILLARYS IMMUNOTYPING" reference 2100, "MINICAP IMMUNOTYPING" reference 2300 and "CAPI 3 IMMUNOTYPING" reference 2600.
Recall Or Safety Alert for Astral 100, Astral 100SC and Astral 150 fans; Astral external batteries and Astral battery packs (spare parts)
Recall Or Safety Alert for AdVance XP male band system, reference 720163-01
Recall Or Safety Alert for Module Cobas c 501 yc 502
Recall Or Safety Alert for Overpressure safety valves of the extra-corporeal tube of Terumo
Recall Or Safety Alert for X-ray tube ceiling unit CH-200 of the FDR Visionary Suite digital radiography system, model MP95A9258004.
Recall Or Safety Alert for Digital mammography system AMULET f / s (FDR MS-2500/2000), AMULET Innovality (FDR MS-3500).
Recall Or Safety Alert for ORTHO BioVue® system (Rh / K cassette)
Recall Or Safety Alert for Head CoCr Affinis 43/15/2 item number 102.02.00.15.0
Recall Or Safety Alert for LIFECODES HLA-DPA1 / B1 SSO, HLA-DRB1 and HLA-DQA1 / B1 Typing KitS
Recall Or Safety Alert for Test N Human Antiserum Ig / L-chain, Lambda type (urine application), product code OWHH09, Siemens material number (SMN) 10446596.
Recall Or Safety Alert for Cardiac Implantable Cardioverter Defibrillators (ICDs) and Defibrillators with Cardiac Resynchronization Therapy (CRT-Ds), Platinium models.
Recall Or Safety Alert for DIAQUICK H.pylori Cassette Catalog No.: Z06229CE, MEZ06229CE, Z98229B
Recall Or Safety Alert for Alere HIV Combo
Recall Or Safety Alert for Prismaflex control units
Recall Or Safety Alert for Mural shots of carbon dioxide (CO2) / oxygen (O2).
Recall Or Safety Alert for Percuvance® Percutaneous Surgical System
Recall Or Safety Alert for Percuvance® Percutaneous Surgical System
Recall Or Safety Alert for Monitor / defibrillator LIFEPAK 12 and LIFEPAK 15, with final expiratory CO2 function (EtCO2), model V15-5-000XXX and catalog number 99577-00XXXX.
Recall Or Safety Alert for Ipsogen kit BCR-ABL1 Mbcr IS-MMR (24), REF 670723, kit ipsogen BCR-ABL1 Mbcr IS-MMR DX, REF 670823 and kit ipsogen BCR-ABL1 Mbcr RGQ RT-PCR, REF 670923.
Recall Or Safety Alert for Femoral cutting guide of partial knee prosthesis Person (size 8), references 42-5781-008-01 and 42-5781-008-02.
Recall Or Safety Alert for Synchronism cables M1783A and M5526A used with HeartStart Mrx, XL and XL + monitors / defibrillators
Recall Or Safety Alert for Phadia 1000 immunoassay analyzer, item number 12-3800-01, including all versions of ISW software (originally submitted as UniCAP 1000 or ImmunoCAP 1000)
Recall Or Safety Alert for Sysmex DI-60, Reference 07115709001
Recall Or Safety Alert for Imaging systems SPECT, SPECT.CT, PET, PET.CT of SIEMENS
Recall Or Safety Alert for AIRO Mobile CT System. Model MobiCTTM-32.
Recall Or Safety Alert for Artis, X-Workplace, Sensis and Arcadis systems with outdated hardware or software.
Recall Or Safety Alert for Traumatology instruments, MINI QUICK ANCHORING BIT 1.0 mm and MINI DRILL BIT 1.1mm QUICK ANCHOR
Recall Or Safety Alert for Reaction assays of NADH and / or NADPH affected by the interference with Sulfasalazine and Sulfapyridine used in the ADVIA Chemistry Systems, Dimension / Vista Dimension Systems and Syva EMIT Systems.
Recall Or Safety Alert for Reusable electrodes Nitinol RF (TCN) models TCN-5-3M, TCN-10-3M, TCN-15-3M, TCN-5, TCN-10, TCN-15, TCN-20, TCNK-5, TCNK-5- C, TCNK-10, TCNK-10-C, TCNK-15, TCNK-15-C, TCNK-20
Recall Or Safety Alert for X-ray system "RadRex-i"
Recall Or Safety Alert for ADVIA Centaur BR reagent (CA 27.29) with lots of Multidiluent 1 finished in 2577 and all future batches
Recall Or Safety Alert for Ophthalmic gases Perfluoropropane sulfur and sulfur hexafluoride.
Recall Or Safety Alert for Anesthesia equipment WATO EX-65, WATO EX-55, A5 and A7
Recall Or Safety Alert for Consoles of intra-aortic counterpulsation (BCIA), distributed between 4-03-2003 and 16-6-2017: • CS100i BCIA, reference 0998-UC-0446HXX; 0998-UC-0479HXX • CS100 BCIA, reference 0998-00-3013-XX; 0998-UC-3013-XX • CS300 BCIA, reference 0998-00-3023
Recall Or Safety Alert for VITROS Chemistry Products Performance Verifier II, product code 8231474
Recall Or Safety Alert for Class I lyophilized supplement, reference CABC-1D
Recall Or Safety Alert for Oxoid ™ GC Agar, reference CM0367 (B, R, T, Q, K)
Recall Or Safety Alert for BacT / ALERT® BPN culture flasks, Reference 279045
Recall Or Safety Alert for KickStand pins and 2.8mm locking bit guide
Recall Or Safety Alert for ORA® system with VerifEye® model 8065998300.
Recall Or Safety Alert for Euphora ™ and Solarice ™ semidistensible rapid exchange dilation balloon catheters.
Recall Or Safety Alert for FluoroType® CDiff kit analyzer VER 1.0.
Recall Or Safety Alert for Clamp for long and short spinous process (Models 9734715 and 9734716) and double clamp for long and short spinous process (Models 9734723 and 9734724).
Recall Or Safety Alert for JTS growth drive unit, catalog number MLE3
Recall Or Safety Alert for SSP AllSet + ™ Gold kits.
Recall Or Safety Alert for Sicuro Plus electric bed, model 5369, references 146562 and 114787
Recall Or Safety Alert for Elecsys Digoxin test used in the cobas e 801 immunoanalyzer.
Recall Or Safety Alert for Syngo Workflow MLR systems that use the Radiologist Portal.
Recall Or Safety Alert for SoKINOX nitrogen oxide supply and control system reference 66 94 550 and SERViNO NO (nitric oxide) reference 68 81 700.
Recall Or Safety Alert for Guide needles 70 cm. See affected references in the notice of the company.
Recall Or Safety Alert for MOSAIQ® system used with linear accelerators with the RATM license
Recall Or Safety Alert for NovoPen® Echo® insulin pen cartridge holders, lot no. DVG1564-6, EVG2298-2, EVG2914-4, EVG3011-4, EVG4140-1 and FVG7571-1
Recall Or Safety Alert for Modular Analytics <E170> Modular Analytics EVO <E170> Module cobas e 601 Module cobas e 602
Recall Or Safety Alert for Modular Analytics <E170> Modular Analytics EVO <E170> Module cobas e 601 Module cobas e 602
Recall Or Safety Alert for Surgical microscopes "Leica M525 F40"
Recall Or Safety Alert for 30ATM inflation device, reference 12-003704
Recall Or Safety Alert for 30ATM inflation device, reference 12-003704
Recall Or Safety Alert for LANTIS oncology information system
Recall Or Safety Alert for Endoprotesis Vascular Toracica Zenith Alpha ™
Recall Or Safety Alert for Plum 360 Infusion Pumps, reference 30010, manufactured between April 29, 2015 and October 25, 2016, and distributed before May 1, 2017
Recall Or Safety Alert for Coulter analyzers LH 750, LH 780, LH 500, HmX CP, HmX AL
Recall Or Safety Alert for ARTISET HD DNL HC blood line, code 955364.
Recall Or Safety Alert for TomcatTM instrument, references ASY-07379 and RASY-07379.
Recall Or Safety Alert for EMBLEM ™ S-ICD programmer, model 3200
Recall Or Safety Alert for EMBLEM ™ S-ICD programmer, model 3200
Recall Or Safety Alert for EMBLEM ™ S-ICD programmer, model 3200
Recall Or Safety Alert for Flowtron Compressor ACS900
Recall Or Safety Alert for ASP6025 tissue processor
Recall Or Safety Alert for ASP6025 tissue processor
Recall Or Safety Alert for S-ICD systems: SQ-RXTM model 1010, EMBLEMTM model A209 and EMBLEMTM MRI model A219.
Recall Or Safety Alert for Nano Humeral Comprehensive Component
Recall Or Safety Alert for Cockpits with revision index 06 or higher that contain 4 GB RAM modules used with Infinity® Acute Care systems and Upgrade Kits that include 4 GB RAM modules
Recall Or Safety Alert for Analyzers for immunochemistry: cobas e 411 and Elecsys 2010
Recall Or Safety Alert for Vue Optic ™ visualization source, reference FVO-150, and Flexor® Vue ™ baffle endoscopic system, references FV-090075-150 and FV-090045-150.
Recall Or Safety Alert for HexaPOD evo RT system with iGUIDE® 2.2
Recall Or Safety Alert for Set Barrier®, references 60611-01, 60612-01, 60614-01, 60615-05, 60205-01, 60302-01, 698780-08, 699175-08, 699180-08
Recall Or Safety Alert for BK Virus R-gene®
Recall Or Safety Alert for Clinical oncology system MOSAIQ.
Recall Or Safety Alert for Products of Digital Sanitary Services and Products Syngo Healthineers of Siemens
Recall Or Safety Alert for Cordless heart pacemaker NanostimTM, model LSP102
Recall Or Safety Alert for Stationary X-ray Artis digital angiography systems, used together with the Artis table.
Recall Or Safety Alert for Philips DuraDiagnost X-ray systems, models 712211 and 712210
Recall Or Safety Alert for Catheter extraction ball Extractor Pro RX-S
Recall Or Safety Alert for Ultrasonic diagnostic system and Ultrasonic work stations of the Xario and Aplio range.
Recall Or Safety Alert for Radifocus Introducer II, Radifocus Introducer II M Coat and Glidesheath Slender
Recall Or Safety Alert for Multirate infusers and regional analgesia
Recall Or Safety Alert for Implants for traumatology
Recall Or Safety Alert for Output Unit (Output Unit) of the Cobas® Connection Modules (CCM), reference 07667574001
Recall Or Safety Alert for VITEK® 2 susceptibility cards
Recall Or Safety Alert for X-ray mobile system DRX-Revolution
Recall Or Safety Alert for Aortic cannulae models RA-1XXX, NA-1XXX, manufactured from June 2014 to April 13, 2017.
Recall Or Safety Alert for Heating head of the Incubator Systems "Ohio Infant Warmer Systems (IWS)". Models: 2001 from IWS (international), 3000 IWS, 3050 IWS, 3100 IWS, 3150 IWS, 3300 IWS, 3500 IWS, 4000 IWS, 4300 IWS, 4400 IWS, 5000 IWS, 3051 IWS and 3400 IWS.
Recall Or Safety Alert for Negative pressure units HARTMANN VivanoTec® and ATMOS® S 042 NPWT
Recall Or Safety Alert for Roof tube bracket CH-200 of the Shimadzu RADspeed Pro X-Ray System.
Recall Or Safety Alert for Manual resuscitation systems, BVM (Bag- Valve- Mask)
Recall Or Safety Alert for LX3 Microscope Floor Stand used with LuxOR ™ Ophthalmic Microscope and LuxOR ™ Ophthalmic Microscope with Q-VUE 3D Visualization Assistant.
Recall Or Safety Alert for Sample preparation systems PrepPlus and PrepPlus 2, references 286600 and 378600
Recall Or Safety Alert for MULTIGENT Creatinine reagent (Enzymatic), reference numbers 8L24-31 and 8L24-41
Recall Or Safety Alert for OSTEOTOME BLADES
Recall Or Safety Alert for Multifunctional Holmium Laser Fibers from Cook
Recall Or Safety Alert for Zurpaz ™ Directional Pods: 8.5F Asymmetric Curve, reference M004EPTMCA85400, Lot 363848 and 8.5F Symmetric Curve, reference M004EPTMC85300, Lot 384797
Recall Or Safety Alert for DxH 500 system
Recall Or Safety Alert for Needle for incision / SBK biopsy. (Cutting biopsy needles) Codes 17030050, 17030070, 17030080 and 17030100.
Recall Or Safety Alert for Exactech Logic Fit tibial impactor head instrument.
Recall Or Safety Alert for Pereyra-Raz ligature holder (Pereyra-Raz Ligature Carrier), Pereyra '75 ligature holder (Pereyra-Raz Ligature Carrier) and Stamey needle (Stamey Needle).
Recall Or Safety Alert for Standard N Protein SL and N / T Protein Control SL.
Recall Or Safety Alert for Perfusion System Module Normo / hypothermia 3T
Recall Or Safety Alert for D2RS X-ray Remote Control Tables, VISIONARY DRF and DX-D800 models
Recall Or Safety Alert for Guide tip of the caliper Exactech Novation, catalog no. 161-00-30
Recall Or Safety Alert for Pilot end mills modular and non-modular Equinoxe
Recall Or Safety Alert for Werber cannulated countersink for CBS microtunnels, round shank, Art. No. 503004341 and AO shank, Art. No. 503004541.
Recall Or Safety Alert for SHUNTASSISTANT, model FV253T
Recall Or Safety Alert for ETEST®OX 256 (OXACILLIN) Presentation Foam reference 520518.
Recall Or Safety Alert for Neuromuscular transmission cables (NMT) Philips IntelliVue with code 989803174581 manufactured between July 2012 and December 2015.
Recall Or Safety Alert for Respironics V60 fans manufactured before September 15, 2015
Recall Or Safety Alert for X-ray systems DigitalDiagnostics
Recall Or Safety Alert for Cobas MPX tests for use in Cobas® 6800/8800 systems
Recall Or Safety Alert for Microgenics test application sheets for extended use in different analyzers. See the trials and platforms affected in the annex to the notice of the company.
Recall Or Safety Alert for ETEST® ETP32 (Ertapenem), reference 531600
Recall Or Safety Alert for Minimed 640G Insulin Infusion Pump
Recall Or Safety Alert for Minimed 640G Insulin Infusion Pump
Recall Or Safety Alert for Flocare® gastrostomy replacement tube (G-tube) with ENFit connector
Recall Or Safety Alert for SONIC 1.5F Microcatheter
Recall Or Safety Alert for Assay buffer 17-OHP, lot 653513, included in the AutoDELFIA Neonatal 17a-OH-progesterone kit
Recall Or Safety Alert for VIDAS® FT4, reference 30459, lot no. 1005291190
Recall Or Safety Alert for Anesthesia system Carestation 620, 650, 650c
Recall Or Safety Alert for Endo Peanut ™ 5mm blunt dissector
Recall Or Safety Alert for Caliper Dimension Vista PROT1 CAL and controls PROT1 CON (L & M & H).
Recall Or Safety Alert for Various Cook products
Recall Or Safety Alert for Left Ventricular Assist System (LVAS) HeartMate 3 ™, reference 106524INT - LVAS KIT, HM 3
Recall Or Safety Alert for Extension for infusion pumps. Reference. TR-26.
Recall Or Safety Alert for Access Total T3 reference 33830, Access Thyroglobulin reference 33860, Access GI Monitor reference 387687, Access Free T4 reference 33880
Recall Or Safety Alert for EMAG® system, reference 418591
Recall Or Safety Alert for NT-proBNP reagent pack from VITROS® Immunodiagnostic Products (10758750002061), product code 6802156, lot 1620
Recall Or Safety Alert for OptilLite ™ Optical Fibers Holmium Laser (Multi Purpose), catalog numbers HLF-M273-CNV, HLF-M273-SMA, HLF-M365-CNV, HLF-M365-SMA, HLF-M550-CNV, HLF-M550-SMA, HLF-M940-CNV, HLF-M940-SMA
Recall Or Safety Alert for Navlock tracking device, kits and related sets.
Recall Or Safety Alert for Gas cartridges for the gas analyzer RAPIDLab® 348 and RAPIDLab® 348EX
Recall Or Safety Alert for KYPHON® Directional Bone Filler Model F04C
Recall Or Safety Alert for Implantable Cardiac Resynchronization Defibrillators (CRT-D) Claria MRI CRT-D SureScan and Wide MRI CRT-D SureScan.
Recall Or Safety Alert for SET MINI RYTHMIC PN WITH PUNZON DEHP FREE, Reference KM1.EE.148.0.
Recall Or Safety Alert for Polysorb ™ Braided Absorbable Suture, Endo Stitch ™ Loading Unit with Polysorb ™ Suture
Recall Or Safety Alert for VERSAJET II Hydrosurgery System Console, product code 66800039
Recall Or Safety Alert for Laboratory Automation Systems enGen ™ version 4.2 TCAutomation software, Rack exit module, ref 952019-EG, Rack entry / exit module (combined), ref 952020, Stago STA-R interface module from Thermo Scientific
Recall Or Safety Alert for VidimSoft OrthoScan ™ system, code 300.0122 ORTHO ™ and Workstation for BioVue® cassettes, code 6904629
Recall Or Safety Alert for Microparticle chemiluminescence immunoassay (CMIA) for the quantitative determination of free thyroxine (Free T4) in human serum or plasma.
Recall Or Safety Alert for Needles for tattoo
Recall Or Safety Alert for UniCel DxH 600/800 Coulter Cellular Analysis System
Recall Or Safety Alert for Stealth Chamber, parts No. DS50-001-XL-T, DS50-002-XL-T, DS50-003-XL-T, DS50-102-XL-T, DS50-103-XL-T
Recall Or Safety Alert for Ophthalmic Viscosurgical Devices (DVO): Healon, Healon GV, Healon 5 Pro and Healon Pro. Models 10200011, 10200012, 10200014, 10201012 and 10201014.
Recall Or Safety Alert for Venture RX catheter (model 5820), Venture OTW catheter (model 5821) and Venture CS catheter (model 5822).
Recall Or Safety Alert for Identification cards and VITEK® 2 Antibiogram.
Recall Or Safety Alert for Ophthalmic solution Goniovisc 2.5%, 15ml
Recall Or Safety Alert for Emminens eConecta
Recall Or Safety Alert for Monopolar high frequency resection electrodes, model A22201A, A22201C, WA22037C.
Recall Or Safety Alert for PAK needles (pedicle access kit). Model 8670009
Recall Or Safety Alert for Omega standard drive screw 110 mm in length, batch no. V06279 and Omega standard drive screw 105 mm in length, batch no. V06269
Recall Or Safety Alert for Stamey Needle, Clarke-Reich Laparoscopic Knot Pusher, Endoscopic Introducer / Extractor, Pereyra Ligature Carrier '75 ®, Pereyra-Raz Ligature Carrier ™.
Recall Or Safety Alert for LABScreen® Multi, Catalog ID LSMUTR
Recall Or Safety Alert for Defibrillator / Monitor Efficia DFM100, model code 866199
Recall Or Safety Alert for VITROS 250 and 350 Chemistry System with software version 9.5
Recall Or Safety Alert for ARROW® kits that include BD Eclipse ™ needles
Recall Or Safety Alert for Access BR Monitor Trial, reference 387620, used with the immunoassay systems of the Access family
Recall Or Safety Alert for Inflation system DOLPHIN
Recall Or Safety Alert for Neuro Stereotactic System | mate® used with Voxim® software
Recall Or Safety Alert for EP-TRACER
Recall Or Safety Alert for ADVIA Centaur Insulin Calibrator and ADVIA Centaur Insulin ReadyPack
Recall Or Safety Alert for Syringe pumps AlarisTM GS, GH, CC, TIVA, PK, Enteral and syringe pumps AsenaTM GS, GH, CC, TIVA, PK
Recall Or Safety Alert for ACOR® hip-strap of modular intention and modular neck INTEGRALE®. Replacement hip stem OPTIMAL® with modular neck.
Recall Or Safety Alert for Disposable devices for hyperthermic perfusion treatments
Recall Or Safety Alert for Allura XperFD and Allura CV20 intervention systems with the "Laird chiller" refrigerator, identification code 98960021599.
Recall Or Safety Alert for Sensis systems (AXIOM Sensis)
Recall Or Safety Alert for Femoral stems LINE
Recall Or Safety Alert for Pulsante® sphenopalatine ganglion micro-stimulator system.
Recall Or Safety Alert for Rechargeable Li-ion batteries used in Beneview T1 patient monitors
Recall Or Safety Alert for Header Monitors Life Scope G9 series, model CSM-1901
Recall Or Safety Alert for Spheres (strawberries) diamond with coarse and extra-coarse grains
Recall Or Safety Alert for Olympus Duodenoscope TJF-145.
Recall Or Safety Alert for Synchromed II implantable drug infusion pump, Model 8637, with pumps manufactured before June 2011
Recall Or Safety Alert for Reagents ACHITECT SHBG, references 8K26-20 and 8K26-25
Recall Or Safety Alert for Miele washer-disinfector, models PG 8527, 8528, 8535 and 8536.
Recall Or Safety Alert for Newport TM HT70 and Newport TM HT70 Plus respirators.
Recall Or Safety Alert for RAPID Point® 500 Blood gas analyzer, SMN (Siemens Material Number) 10492730, 10696857, 10697306.
Recall Or Safety Alert for IMMULITE® / IMMULITE® 1000 LBP (Protein that binds to lipopolysaccharide), reference LKLB1, Siemens Material Number (SMN) 10381395.
Recall Or Safety Alert for IMMULITE® 2000 / IMMULITE® 2000 XPi LBP (Protein that binds to lipopolysaccharide), reference L2KLB2, Siemens Material Number (SMN) 10381474.
Recall Or Safety Alert for AQUIOS CL Flow cytometer, reference B30166.
Recall Or Safety Alert for Dialysis systems: ARTIS 230V, product code 110635, EVOSYS 230V, product code 110648 and ARTIS 230V Physio, product code 115323.
Recall Or Safety Alert for Ortho Clinical Diagnostics Inc., USA.
Recall Or Safety Alert for Anatomical Femoral Heads LFIT ™ V40 ™ by CrCo
Recall Or Safety Alert for Radiotransparent Wilson frame pads
Recall Or Safety Alert for Suture Optilene 8/0 (0.4) 60 cm 2xDR8, reference C3090887
Recall Or Safety Alert for Digital insoles for hip spurs Echo® Bi-Metric®
Recall Or Safety Alert for C atraumatic compact cysto-urethroscope of 25º, model 8645403, serial numbers 1100317389, 1100317397 and 1100317401.
Recall Or Safety Alert for Manometer Tray, Jamshidi Biopsy Needle, Illinois Needle (TJ) for aspiration, Jamshidi Needle (TJ) for bone marrow and Thoracentesis / Paracentesis Kit ".
Recall Or Safety Alert for Cholesterol Reagents, Creatinine, HDL Cholesterol, Lactate, Triglycerides, Uric Acid and Salicylate Synchronous Systems
Recall Or Safety Alert for Laboratory Automation Systems enGen ™ using any version of the TCAutomation ™ (TCA) software with the InOut communications interface
Recall Or Safety Alert for NC Trek RX coronary dilatation catheter, NC Traveler RX coronary dilatation catheter and NC Tenku RX PTCA Catheter Balloon
Recall Or Safety Alert for Lot 9251K-E of the Uni-GoldTM H. pylori Antigen assay, reference 1206650
Recall Or Safety Alert for Pentax EB-1970UK ultrasound videobronchoscope, instruction number Z870, revision number R10-R12
Recall Or Safety Alert for Secura Protective Cream Z10 78g, article number 59447525, lot number affected 626110
Recall Or Safety Alert for Compact air gas modules E-CO, E-VOC, E-COVX, E-CAiO, E-CAiOV and E-CAiOVX, serial numbers 6704120 to 6778756
Recall Or Safety Alert for lot 1KR5K1618 of the diagnostic test RESIST-3 OKN K-set
Recall Or Safety Alert for Metal heads: Modular femoral heads (CoCr), Protasul® S30 femoral heads, Metasul® heads; that can be used in a combination metal on polyethylene
Recall Or Safety Alert for Digital linear accelerators of the PRIMUS ™ and MEVATRON ™ types, with serial number less than 3094
Recall Or Safety Alert for Digital linear accelerators of the types ARTISE ™, ONCOR ™ and PRIMUS ™, with serial number from 3094.
Recall Or Safety Alert for Pregnancy rapid test NADAL® hCG Pregnancy, reference 142002
Recall Or Safety Alert for Test INMULITE®2000 / INMULITE® 2000 XPi IgG4 specific allergen
Recall Or Safety Alert for Tibial components of the Total Knee System Triathlon
Recall Or Safety Alert for CMI - Collagen-based meniscal implant, references 4601, 4607 and 4612.
Recall Or Safety Alert for PMH 7000 Humidifier Base.
Recall Or Safety Alert for Analyzers Cobas b 221
Recall Or Safety Alert for Double flat screen monitor stand Chromophare surgical lighting system mounted on ceiling. References: CT 0604004, CT 0604104, CT 0605004, CT 0605104 and CT 0606104.
Recall Or Safety Alert for Fabius anesthesia systems. Models: GS Premium, Shot, DM Shot, MRI, plus, plusXL.
Recall Or Safety Alert for Intrauterine devices (IUD), models: ANCORA, NOVAPLUS® and GOLD T®
Recall Or Safety Alert for 3M ™ Professional Surgical Shaver, Model 9681
Recall Or Safety Alert for Centricity Universal Viewer viewer with PACS-IW foundation 6.0.X and Centricity PACS-IW with version 5.0.X of Universal Viewer with PACS-IW foundation.
Recall Or Safety Alert for Ureterorenal videoendoscopes URF-V2 and URF-V2R Ureterrenal fibersides URF-P6 and URF-P6R
Recall Or Safety Alert for LIVES and mini LIVES
Recall Or Safety Alert for LIFEPAK 20e monitors / defibrillators, manufactured between September 2016 and June 2017
Recall Or Safety Alert for Means for In Vitro Fertilization (IVF)
Recall Or Safety Alert for Bio-Cal Heat Exchanger, Model 370 and 370I
Recall Or Safety Alert for Dornier Gemini
Recall Or Safety Alert for DEA HeartStart FR3 and Monitors / External HeartStart MRx Defibrillators using the cardiopulmonary resuscitation (CPR) or CPR sensor
Recall Or Safety Alert for Carescape Central Station (CSCS2), all-in-one models with GTIN 00840682109666 and desktop with GTIN 00840682109604
Recall Or Safety Alert for Patient positioning system ExacTrac
Recall Or Safety Alert for Thermo Scientific ™ Oxoid ™ BIGGY Agar 500g CM0589B culture medium
Recall Or Safety Alert for CADD ™ medication reservoir cassettes (no flow interruption) with codes 21-7001-24, 21-7002-24 and 21-7100-24.
Recall Or Safety Alert for PA023E probe used in MyLab Ultrasound Diagnostic Systems
Recall Or Safety Alert for Ultrasonic diagnostic systems, references 1016200xx, 1016250xx, 9806100xxx and 9806150xxx in ElaXto mode (sonoelastography application) activated
Recall Or Safety Alert for ProGrade systems
Recall Or Safety Alert for Intraoperative image system O-arm® 1000 (3rd edition), model BI70000028230
Recall Or Safety Alert for RayStation 4.9 (RayPlan 1), RayStation 5, RayStation 6 (RayPlan 2) and RayStation 7 (RayPlan 7)
Recall Or Safety Alert for OASIS.
Recall Or Safety Alert for Suction hoses for XO 4 and XO FLEX Dental Units
Recall Or Safety Alert for Suction hoses for XO 4 and XO FLEX Dental Units
Recall Or Safety Alert for Aurinio operating room luminaires of the L 110, L 120, L 150 and L 160 series.
Recall Or Safety Alert for Cortisol Saliva ELISA, code RE52611
Recall Or Safety Alert for Flex® Calcium Reagent Cartridge for the Dimension Vista® System, catalog number K1023 and Siemens Material Number (SMN) 10445160
Recall Or Safety Alert for Bag with hemodialysis concentrate, reference SAK-304, for use with Pureflow SL.
Recall Or Safety Alert for Invia Motion, reference 087.4022 and 087.4024.
Recall Or Safety Alert for Syngo Workflow MLR, all versions.
Recall Or Safety Alert for Allura Xper Systems, Allura Clarity, Allura CV, Allura Centron and Integrity
Recall Or Safety Alert for STRAUSS PENIS CLAMP 130MM Model EF401R.
Recall Or Safety Alert for KIT BORRELIA VIRCLIA® IgG MONOTEST, Reference VCM009, lot 17C009005
Recall Or Safety Alert for Introducer PLIS. Reference: PLIS008.
Recall Or Safety Alert for Cemented Troquelar implants SIGMA® HP PFJ.
Recall Or Safety Alert for External defibrillators REANIBEX 300 and REANIBEX 500
Recall Or Safety Alert for Bone Cement Optipac 40 Refobacin Revision, reference 4730501163-1
Recall Or Safety Alert for Biatain Ibu dressing, item number 3415201011
Recall Or Safety Alert for Carescape R860 fan, Model GTIN # 00840682102346
Recall Or Safety Alert for Ficina solution contained in the Kit Panocell®-10 Ficin-Treated, reference 0002385
Recall Or Safety Alert for Gastrointestinal lining system EndoBarrier® with implantation system, reference 40-10-00364
Recall Or Safety Alert for Philips Patient Monitoring Center IntelliVue Information Center (PIIC) iX
Recall Or Safety Alert for Volumetric infusion pumps Syramed μSP6000 and Volumed μVP7000
Recall Or Safety Alert for 3M ™ Bair Hugger ™ Warming / Cooling Blanket, Thermal Blanket, Model 63500
Recall Or Safety Alert for TL-HEX double-row standing bows sterilized, all sizes
Recall Or Safety Alert for BD Vacutainer® SST ™ II Advance Plus blood collection tubes, reference 368879.
Recall Or Safety Alert for Dental Implants SwishPlus and SwishTapered
Recall Or Safety Alert for BrightView, BrightView X, BrightView XCT, Precedence 6 and Precedence 16 image systems.
Recall Or Safety Alert for Allura Xper endoluminal intervention system
Recall Or Safety Alert for Flow cytometry system COULTER®EPICS® XLTM and COULTER EPICS XL-MCLTM with Software System II; • FC 500TM series flow cytometry system, all software versions (new, reconditioned or restored)
Recall Or Safety Alert for Alcon TOTALPLUS® 25 + ® Vitrectomy Pak, reference no .: 8065751617, batch no. 2060953H (included as a component in the Custom Pak® for ophthalmic surgical procedure, catalog no. C25366-01, batch no. 507664)
Recall Or Safety Alert for Kit therascreenKRASPyro (24) 971460, kit therascreenBRAFPyro (24) 971470, kit therascreenEGFRPyro (24) 971480, kit therascreenGISTRapidScreenPyro 971510, kit therascreenNRASPyro (24) 971530, kit therascreenRASExtPyro 971590, reagents PyroMarkGoldQ24 971802
Recall Or Safety Alert for Stationary x-ray system of digital angiography AXIOM Artis with a flat detector of a batch of specific production.
Recall Or Safety Alert for Digital radiography system DRAD-3000E (RadRex-i)
Recall Or Safety Alert for Confidence Cement System Kit
Recall Or Safety Alert for BD Phoenix Gram Negative panels with colistin.
Recall Or Safety Alert for CellaVision DM96, CellaVision DM1200, CellaVision DM9600 and remote review software CellaVision
Recall Or Safety Alert for Custom implant systems with the non-invasive growth component (MIG) manufactured between March 2007 and October 2014.
Recall Or Safety Alert for VOLISTA surgical lamps, StandOP, Triop and Access models, manufactured before July 2016.
Recall Or Safety Alert for MARS Treatment Kit, Type 1116/1-X-MARS. Code: 800540
Recall Or Safety Alert for Guider Softip ™ XF guide catheters
Recall Or Safety Alert for Test humerus stems of the TITAN TM total modular shoulder system (TSS).
Recall Or Safety Alert for END BALL intragastric balloon system, reference ENDT110
Recall Or Safety Alert for DxH 500 system, reference B40601
Recall Or Safety Alert for Anesthesia systems 9100c and Aelite
Recall Or Safety Alert for ADVIA Centaur, ADVIA Centaur CP, ADVIA Centaur XP and ADVIA Centaur XPT systems
Recall Or Safety Alert for Highly polished hip and knee implants packed in a low density polyethylene (LDPE) bag.
Recall Or Safety Alert for iQ-X 2.2.0 (with valid software license), iQ-WEB ≤ 6.4.5 (only when used in connection with a licensed iQ-X 2.2.0), iQ-4VIEW ≤ 2.0 (only when used in connection with a licensed iQ-X 2.2.0).
Recall Or Safety Alert for DU893 portable dental unit; Benmayor codes: APC000600 and APC000650
Recall Or Safety Alert for Urine analyzer Cobas u 601, reference 06390498001, and Cobas u 701 analyzer, reference 06390501001.
Recall Or Safety Alert for Prelude SNAP ™ split pod introducer
Recall Or Safety Alert for Titanium DS clips for ligature.
Recall Or Safety Alert for Manual Resuscitation Systems, BVM (Balloon-Valve-Mask)
Recall Or Safety Alert for 2M 15 ° insert for LUMiC® and RS cup of the MUTARS® revision system (Modular Universal Tumor and Revision System) with titanium nitride coating.
Recall Or Safety Alert for Bulkamid, product no. 50047
Recall Or Safety Alert for MacoGenic Set XUV8501Q.
Recall Or Safety Alert for PORT-A-CATH® deposit kits and Power Introducer PORT-A-CATH® II
Recall Or Safety Alert for MTX® fully coated dental implant ™ (Tapered Screw-Vent model)
Recall Or Safety Alert for VACUETTE® FC Mix tube
Recall Or Safety Alert for Systems ADVIA Centaur CP, ADVIA Centaur XP and ADVIA Centaur XPT.
Recall Or Safety Alert for TruVidiaTM wireless receiver. Model 1940747
Recall Or Safety Alert for Pentacam® AXL
Recall Or Safety Alert for Control pedal S-N1 / S-N2. These pedals were delivered together with surgical units W & H Implantmed and W & H Elcomed manufactured between March 2016 and September 2017, as well as individually as an accessory.
Recall Or Safety Alert for SMR grafting blade (Product code 9013.75.443)
Recall Or Safety Alert for I walk V2.0.
Recall Or Safety Alert for Xpert® GBS reference GXGBS-100N-10
Recall Or Safety Alert for Staple gun (clips), models CG8900, CG8901, CG8901A
Recall Or Safety Alert for OptiView DAB IHC Detection Kit, UltraView Universal DAB Detection Kit, CINtec PLUS Cytology Kit, OptiView Amplification Kit, OptiView Amplification Kit (250 tests), Hematoxylin II
Recall Or Safety Alert for Website software TAYLOR SPATIAL FRAME.
Recall Or Safety Alert for Cordis® SMART® Flex Vascular Stent System.
Recall Or Safety Alert for Allergen c5 ImmunoCAP, Ampicillin, item number 14-4450-01; Allergen c6 ImmunoCAP, Amoxicillin, item number 14-4451-01
Recall Or Safety Alert for Hemoglobin A1c reagent (HbA1c), reference 4P52-21, used with Architect 4000 and 8000 systems
Recall Or Safety Alert for Adjustable gastric band LAP BAND. Code C-20360.
Recall Or Safety Alert for Xpert® HIV-1 Viral Load
Recall Or Safety Alert for Spotchem II Glucose, Spotchem II Panel-1, Spotchem II Panel-V and Spotchem II Panel-V2
Recall Or Safety Alert for Signia electric handle. Article code: SIGPHANDLE
Recall Or Safety Alert for Access catheter and SpyScopeTM DS introducer
Recall Or Safety Alert for CELL-DYN Emerald 22 analyzer, reference 09H59-01
Recall Or Safety Alert for Pacemakers, pacemaker and cardiac resynchronization systems (CRT-P): VALITUDE ™ CRT-P, ACCOLADE ™ Pacemakers, ESSENTIO ™ Pacemakers, VISIONIST ™ CRT-P, PROPONENT ™ Pacemakers, ALTRUA ™ 2 Pacemakers
Recall Or Safety Alert for Pacemakers (TRC-P) and defibrillators (TRC-D) for cardiac resynchronization therapy (CRT): TRC-M VALITUDE ™, TRC-D RESONATE ™, TRC-D MOMENTUM ™, TRC-D AUTOGEN ™, TRC-D INOGEN ™, TRC-M VISIONIST ™, TRC-D VIGILANT ™, CHARISMA ™ TRC-D, DYNAGEN ™ TRC-D, ORIG TRC-D
Recall Or Safety Alert for Tests INMULITE®, INMULITE® 1000, INMULITE® 2000, INMULITE® 2000 XPi
Recall Or Safety Alert for Urine analyzer Atellica UAS 800, Reference 11065004
Recall Or Safety Alert for Phadia Prime software up to version 2.1.4 included, when connected to the Phadia 250, Phadia 2500E / EE and Phadia 5000E / E + E instruments
Recall Or Safety Alert for ETEST Teicoplanin 256 (TP) SPB and Foam presentation, references 412461 and 522018.
Recall Or Safety Alert for Digital linear accelerator with detector XVI and iViewGT ™.
Recall Or Safety Alert for ARCHITECT c4000 Cuvette Segment (cuvette segment), reference 02P75-01; ARCHITECT c8000 Cuvette Segment (segment cuvettes) reference 01G46-01; ARCHITECT c16000 Cuvette Segment (segment cuvettes), reference 09D32-05
Recall Or Safety Alert for VITEK®2 AST Gram-Positive cards containing the Cefoxitin Screen test (oxsf01n)
Recall Or Safety Alert for Reagents ARCHITECT DHEA-S, references 8K27-20 and 8K27-25
Recall Or Safety Alert for Reduced energy defibrillation electrodes for children / pediatric use Catalog # 11101-000016 and Nº Min # 3202380-006 and Starter kits Catalog # 11101-000017 and Nº Min # 3202784-009.
Recall Or Safety Alert for Elecsys BRAHMS PCT
Recall Or Safety Alert for Modular Distal Scrap Curve REVITAN®
Recall Or Safety Alert for Contact lenses 1-DAY ACUVUE® MOIST
Recall Or Safety Alert for Norm-Ject tuberkulin syringe, reference K-ATS-1000.
Recall Or Safety Alert for BD Vacutainer® C & S urine tube with preservative. Catalog number: 364958
Recall Or Safety Alert for Better Care Net Server software used with the Dräger Infinity MView patient monitoring solution.
Recall Or Safety Alert for Conventional Hemodialysis Lines (HD)
Recall Or Safety Alert for Dental implants Tapered Screw-Vent, references TSVTB10 and TSV4B10.
Recall Or Safety Alert for Rechargeable lithium-ion batteries with SKU: 10086042, used in Puritan Bennett ™ 980 respirators
Recall Or Safety Alert for Artis systems used with an Artis table.
Recall Or Safety Alert for Multirall ™ 200 (3130001) and car S65 (3136011).
Recall Or Safety Alert for SmartBase electric patient lift, model 9934100
Recall Or Safety Alert for Synchromed® II implantable drug infusion pump, models 8637-20 and 8637-40, with expiration date equal to or before December 31, 2018 (2018-12-31)
Recall Or Safety Alert for Malecot Nephrostomy Catheter System, Malecot Nephrostomy Catheter Set, Re-EntryTM Malecot Nephrostomy Catheter Set and Percutaneous Access Set.
Recall Or Safety Alert for High performance stretchers for TomoTherapy patients.
Recall Or Safety Alert for Premicath PICC Neonatal with detachable needle, Codes 1261.153, 1261.203, 1261.205, 1261.206, 1261.208, 1261.306, 1261.307, 6261.203, 6261.206 and 6261.306
Recall Or Safety Alert for Monoclonal Mouse Anti-Human CDX2, Clone Dak-CDX2, code number M3636
Recall Or Safety Alert for Gelsoft ™, Gelsoft ™ ERS, Gelsoft ™ Plus, Gelsoft ™ Plus ERS, Gelseal ™, Gelseal ™ ERT, Gelweave ™, K-Thin, K-Thin ERS and Gelseal ™ Plus, Fluoropassiv ™, Fluoropassiv ™ ER, Fluoropassiv thin wall and Fluoropassiv ER thin wall, Cardiovascular tissue patches,
Recall Or Safety Alert for Ceramic Femoral head 28 mm outside diameter.
Recall Or Safety Alert for Philips Volcano s5i, CORE and CORE Mobile systems, manufactured between March 23, 2016 and October 18, 2017.
Recall Or Safety Alert for Vascular Access System Vital-Port® Cook
Recall Or Safety Alert for Sysmex DI-60 and CellaVision DM1200
Recall Or Safety Alert for Radial head system rHead and Uni-Elbow
Recall Or Safety Alert for NIM-ECLIPSE® System and disposable stimulation probes of the NIM-ECLIPSE® System
Recall Or Safety Alert for CLINITEK Novus® with Atellica® UAS 800, reference 11046553
Recall Or Safety Alert for RayStation 3.5, 4.0, 4.5, 4.7, 5, 6, RayPlan 1 (RayStation 4.9) and RayPlan 2 (RayStation 6).
Recall Or Safety Alert for Medication Cassette CADD ™ reservoir (without flow interruption) with codes 21-7001-24, 21-7002-24 and 21-7100-24.
Recall Or Safety Alert for System calibrator, reference no. 66300 from Beckman Coulter Creatinine OSR6x78 Method A.
Recall Or Safety Alert for Refobacin bone cement, optipac Refobacin
Recall Or Safety Alert for Kit MuSK-Ab ELISA, reference RE51021, lot EMU124
Recall Or Safety Alert for • RÜSCH Sensor (Series 400) silicone • RÜSCH Non-sterile rectal / pharyngeal temperature sensor.
Recall Or Safety Alert for Polyvalent binder serum of Shigella sonnei (Phases 1 and 2) Thermo Scientific ™ Remel ™, product code R30164201
Recall Or Safety Alert for Alinity i processing module, reference 03R65-01 and Cable, power socket, TED CNTRLER (thermoelectronic device), reference A- 35006203-01
Recall Or Safety Alert for Connection cable, model 2069-CE
Recall Or Safety Alert for Dental products
Recall Or Safety Alert for Electric hospital beds Multicare
Recall Or Safety Alert for Fabius anesthesia systems, GS / GS Premium, MRI, Tiro, Plus / Plus XL models with external fresh gas outlet (ACGO)
Recall Or Safety Alert for Contact lenses: • ACUVUE® ADVANCE®, • ACUVUE® OASYS®, • 1-DAY ACUVUE® MOIST® for ASTIGMATISM®
Recall Or Safety Alert for ACUVUE® OASYS contact lenses for astigmatism
Recall Or Safety Alert for Elekta Linear Accelerators with Integrity R1.2 and Integrity R3.2 operating systems with a Precise Treatment Table ™ for the option licensed with ATM (Automatic Table Movement).
Recall Or Safety Alert for Several models of Videobronchoscope, Sonographic Bronchoscope, Videonasopharyngolaryngoscope and Videocistoscope PENTAX
Recall Or Safety Alert for Intestinal nutrition probe Freka®, ENFit references 7755646 and 7755647
Recall Or Safety Alert for BARRIER® Ultimate Surgical Gown, references 6801021-01, 680103-01, 680104-01, 6801041-01, 6801051-01, 6801061-01, 690102-01, 6901021-01, 690104-01, 6901041-01
Recall Or Safety Alert for Urine microscopy analyzer of the IQ200 series with bar code reader model NFT-2100.
Recall Or Safety Alert for iChemVELOCITY Urine Chemistry Strip, catalog number 800-7204, with expiration date 30/08/2018.
Recall Or Safety Alert for Anaconda ™ long iliac branch endovascular graft system (including straight, flared and tapered configurations).
Recall Or Safety Alert for Monitor / Defibrillator SCHILLER model DEFIGARD Touch7, configured in manual defibrillation mode.
Recall Or Safety Alert for Introducing Intro-Flex® with automatic hemostatic valve, model number I300F85.
Recall Or Safety Alert for "TunneLoc" tibial fixation devices of 8, 9, 10 and 11 mm, references 906512, 906513, 906514, 906515, 906532, 906533, 906534, 906535, distributed between August 2011 and December 2016.
Recall Or Safety Alert for Synchromed® II implantable drug infusion pump, models 8637-20 and 8637-40.
Recall Or Safety Alert for Open vial hematology analyzer DxH 500, reference B40601.
Recall Or Safety Alert for Nuclear medicine systems Millennium VG, Discovery VH and VariCam, all configurations.
Recall Or Safety Alert for NanostimTM wireless cardiac pacemaker, model S1DLCP
Recall Or Safety Alert for NanostimTM wireless cardiac pacemaker, model S1DLCP
Recall Or Safety Alert for NanostimTM wireless cardiac pacemaker, model S1DLCP
Recall Or Safety Alert for Computerized tomography equipment SOMATON Force and SOMATOM Definition AS, AS +, Edge and Flash, using the Care Dose4D algorithm.
Recall Or Safety Alert for Impactor pad of partial knee prosthesis Person, Reference 42539909100.
Recall Or Safety Alert for Dual Hemo MCable modules, reference MS20783, with revision index (RI) 15 and 16 used together with the Infinity Acute Care System (IACS) monitoring
Recall Or Safety Alert for LINA Gold Loop
Recall Or Safety Alert for Dimension Vista® Calibrator LOCI 8 CAL, catalog number KC646
Recall Or Safety Alert for Hypothermia / hyperthermia modules HCU 20 and HCU 30.
Recall Or Safety Alert for EluviaTM 150mm and InnovaTM stent systems 180 mm and 200 mm.
Recall Or Safety Alert for Fenestrated needle biopsy forceps references CJ-PATC-23-160A (Ref Izasa Hospital 144CJPATC23160A) and CJ-PATC-23-230-A (Ref Izasa Hospital 144CJPATC23230A).
Recall Or Safety Alert for ThermoScientificTM OxoidTM Mueller Hinton Broth culture medium, reference CM04005B.
Recall Or Safety Alert for Epi proColon Plasma Quick Kit. Catalog No .: M5-02-001
Recall Or Safety Alert for Suction probe cleaning system Bond catalog number CS9100
Recall Or Safety Alert for Pulsavac Plus System
Recall Or Safety Alert for Columbus® System Review
Recall Or Safety Alert for Fluid suction systems Medline - 3L MED-SOFT suction bags.
Recall Or Safety Alert for Low Temperature Sterilization Systems V-PRO 60, distributed between July 31, 2014 and August 17, 2017.
Recall Or Safety Alert for Anesthesia system Carestation 620, 650 and 650c
Recall Or Safety Alert for GMK Hinge System.
Recall Or Safety Alert for Screw Abutment Screw Diamond of the OPRA implant system
Recall Or Safety Alert for Screw Abutment Screw Diamond of the OPRA implant system
Recall Or Safety Alert for Solution of the NeoBase succinylacetone assay, model 3042-0020
Recall Or Safety Alert for Mastoid strawberries, references MBUR5060FRCV, MBUR6060FRCV and MBUR7060FRCV
Recall Or Safety Alert for Punch aortic models 080-271, 080-351, 080-401, 080-403, 080-451, 080-481, 080-501.
Recall Or Safety Alert for Screening Panels: Screening panel 123, Cellbind P3, Cellbind P3-P and Column Screen 123.
Recall Or Safety Alert for STI Multiplex Array Kit, catalog number EV3950A / B, lot no. 8971, 8737, 8632 and 7888
Recall Or Safety Alert for Endoscopes from PENTAX Medical
Recall Or Safety Alert for LASEREDGE ophthalmic knives 1.6mm x 1.8mm Angled Trapezoid, 6 / box SKU # E7600, lot MAVR240
Recall Or Safety Alert for Multiplate® analyzers, reference 06675069001, with software versions 2.04.37 and 2.04.39
Recall Or Safety Alert for Intravascular catheters "CERTOFIX DUO, CERTOFIX TRIO and DRUCAFIX"
Recall Or Safety Alert for Thoracic drains ATRIUM OCEAN, OASIS, EXPRESS and EXPRESS MINI, with expiration date prior to October 2019
Recall Or Safety Alert for PICC BioFlo catheters with PASVTM and ENDEXO valve technology
Recall Or Safety Alert for Lots 2069 GL and 2082 GL of Glucose Standard, included in certain references and batches of Glucose Kits GLUC-PAP
Recall Or Safety Alert for Coronary Guide Galeo Pro
Recall Or Safety Alert for Affinity Fusion® Oxygenator with integrated arterial filter and Cardiotomy / venous reservoir with biocompatible surface Balance, Model BB841
Recall Or Safety Alert for SynReam milling rod 2.5 mm, L 650 mm, sterile, reference 351.709S
Recall Or Safety Alert for Computerized Tomography Systems (CAT), Brilliance iCT models, Brilliance Big Bore Oncology, Brilliance 64, Brilliance 40, Brilliance 16, Brilliance 6 and Ingenuity CT, manufactured between January 1,
Recall Or Safety Alert for Exactech Equinoxe Inverse Shoulder Screw Set, Fixed Angle Set, catalog number 320-20-00
Recall Or Safety Alert for LOTUSTM Edge valve system
Recall Or Safety Alert for System syngo RT Oncologist ™ versions 4.3.SP1, 4.3.138, or 4.3.1_MR2
Recall Or Safety Alert for Crane Invacare Birdie
Recall Or Safety Alert for Reagent CD79b PE
Recall Or Safety Alert for Irrigation solutions ECOLAV 500 ml: • "NaCl 0.9% B. BRAUN EL 500ML WEST", code 3570410; NaCl 0.9% ESTERICLEAN EL 500ML WEST ", code 3570470
Recall Or Safety Alert for Kit for intrathecal anesthesia "SPINOCATH", codes 4517717 and 4517725
Recall Or Safety Alert for CONMED Concept® HeatWave® CS-023 Electrode
Recall Or Safety Alert for "Checkcell", catalog number 002224 and 002225, lot 31864.
Recall Or Safety Alert for TCAutomationTM system configured with the Thermo Scientific centrifuge module and the TCAutomation 3.6.2 software version and earlier
Recall Or Safety Alert for Magnetic resonance systems SIGNA Creator and SIGNA Explorer, manufactured between 11/21/2014 and 07/17/2016
Recall Or Safety Alert for Automatic device "NIO-A"
Recall Or Safety Alert for Absorb ™ Bioresorbable Vascular Scaffold (BVS)
Recall Or Safety Alert for Merge CADstream software, versions prior to 5.2.6
Recall Or Safety Alert for Iris Acrysof® IQ with UltrasertTM Injector System, model no. AU00T0.220, batch no. 12409024
Recall Or Safety Alert for Etest® COLISTIN CO256 WW, Ref. 537300 and 537308
Recall Or Safety Alert for Stationary x-ray Artis digital angiography systems with 19 "real-time display (reference DSHC1914-DC and model number 10656055).
Recall Or Safety Alert for POC systems cobas b 123 <4>, reference 05122287001
Recall Or Safety Alert for ValleylabTM laparoscopic electrodes
Recall Or Safety Alert for Clinical Oncology System MOSAIQ Medical Oncology, version 2.50.05 and above
Recall Or Safety Alert for EXTREME® HAP diaphyseal nail - Without cement, ref. 1-01043xx and Long keel for Total knee prosthesis - A cement, ref. 1-02007xx
Recall Or Safety Alert for QIAsymphony DSP kits
Recall Or Safety Alert for Americot blue neurosurgical sponges ½ "x 1", catalog no. 20-05S, lot 2015/10 AB,
Recall Or Safety Alert for Lumipulse G E2-III immunoreaction cartridges, reference 296011
Recall Or Safety Alert for Reagents Total T4 of VITROS®
Recall Or Safety Alert for Pool lift Splash Pool Lift, model number 300-0000EU and 370-0000EU
Recall Or Safety Alert for Detachable spiral "Target Nano" (Detachable coil Target Nano)
Recall Or Safety Alert for Bard Encor® probes
Recall Or Safety Alert for Novocastra TM lyophilized reagent of mouse monoclonal antibody marker for renal cell carcinoma, product code: 1 ml NCL-RCC, batches: 6036120, 6032345 and 6023543
Recall Or Safety Alert for ARCHITECT STAT High Sensitive Troponin-I
Recall Or Safety Alert for LenSx® Laser Equipment with Corneal Flap Module, catalog number 8065998162
Recall Or Safety Alert for TOPAZ MicroDebrider vaporizers
Recall Or Safety Alert for IChem VELOCITY Urine Chemistry strips used in iChem Systems VELOCITY Automated Urine Chemistry
Recall Or Safety Alert for Endotracheal Tube Venner PneuX PY Disposable (Not compatible with Magnetic Resonance Imaging) References: 901060,901070,901080,901090
Recall Or Safety Alert for Magnetic Resonance Imaging Systems Discovery MR450, MR750, MR750w, Optima MR450w, 1.5 T Signa HDxt, 3.0T Signa HDxt, Signa Vibrant
Recall Or Safety Alert for Innovative 2121IQ and Innova 3131IQ X-ray image acquisition systems.
Recall Or Safety Alert for X-ray cardiovascular imaging systems Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ, Innova 2121IQ, Innova 3131IQ
Recall Or Safety Alert for X-ray cardiovascular imaging systems Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ equipped with a GE electrical panel (PDB)
Recall Or Safety Alert for X-ray detectable laparotomy compresses Curity ™
Recall Or Safety Alert for X-ray cardiovascular imaging systems Advantx, Innova 2000, Innova 2100 IQ, Innova 3100, Innova 3100 IQ, Innova 4100 and Innova 4100IQ, equipped with video monitors in suspension, model 2236709, 2353620, 2223039-2 and 2270677-2
Recall Or Safety Alert for "Universal Viewer", versions 5.0 SP2 and later, and "Centricity Universal Viewer", versions 6.0 and later.
Recall Or Safety Alert for Reactive Strips GlucoMen® LX Sensor
Recall Or Safety Alert for RapidPoint® 500 Measuring Cartridge
Recall Or Safety Alert for CP11410 Autoread Mueller-Hinton Broth W / TES W / Lysed Horse Blood, CP112-10 Mueller-Hinton Broth W / TES W / Lysed Horse Blood, T3462 Sensitivity Cation Adjusted Mueller-Hinton Broth W / TES 100 / Pk. and T3462-10 Sensititre Cation Adjusted Mueller-Hinton Broth W / T
Recall Or Safety Alert for X-ray digital angiographic systems "AXIOM Artis FA, FC, dFA, dFC, dFCM, AXIOM Artis BA, BC, dBA, dBC, dBCM" and "AXIOM Artis MP, dMP" with the version of SW VB23N / P
Recall Or Safety Alert for MEDUMAT Transport respirator (with and without CO2 measurement) with software version 5.X.
Recall Or Safety Alert for IChemVelocity systems using urine strips "iChemVelocity Urine Chemistry", references 800-7204 and 800-7204-001
Recall Or Safety Alert for Magnetic Resonance (MR) Systems Discovery MR750w 3.0T, Discovery MR750 3.0T, SIGNA PET / MR 3.0T, SIGNA HDxt 3.0T, SIGNA HDx 3.0T, SIGNA HD 3.0T, SIGNA Excite 3.0T, SIGNA 3.0T
Recall Or Safety Alert for Birmingham Hip Surface Prosthesis (BHR)
Recall Or Safety Alert for Birmingham Hip Surface Prosthesis (BHR)
Recall Or Safety Alert for WATCHMAN® device for closing the left atrial appendage with the introductory system (OAI) and the WATCHMAN® Access System Access sheath with dilator
Recall Or Safety Alert for Linear Digital Accelerators (LINAC) of type ONCOR ™ and ARTISTE ™, which use the control console with software version 12.0.25 or 13.0.65 and Syngo RT Therapist ™, with software version 4.2.110 or 4.3.SP1 .
Recall Or Safety Alert for XiO RTP System with software version 4.51 or higher
Recall Or Safety Alert for Astraia Software for Women's Health ", versions 1.20, 1.21, 1.22 and 1.23, which is used with the module" Astraia FMF - First Trimester Risk Screening for Trisomy 21 "
Recall Or Safety Alert for Ingenuity TF PET / MR system, configuration ES6600119415
Recall Or Safety Alert for Peripheral insert central vein catheter PICC (peripheral venous catheter), with removable sheath component
Recall Or Safety Alert for Folate-Ascorbic Acid / Diluent Ascorbic Acid, Material Number 10316877 (124975), lot numbers 54942, 56230 and 70673
Recall Or Safety Alert for LX3 ophthalmic microscope floor stand, part number 8065752560, serial numbers 1402548501X to 1502857606X
Recall Or Safety Alert for "Set Thrombectomy AngioJet® Spiroflex®", "Set Thrombectomy AngioJet® SOLENT ™ omni", "Set Thrombectomy AngioJet® SOLENT ™ dista" and "Set Thrombectomy AngioJet® AVX®"
Recall Or Safety Alert for Monitors / Defibrillators HeartStart XL +, model 861290
Recall Or Safety Alert for High-pressure spanners, references 12-001914, 12-002022, 12-002023, 12-002024
Recall Or Safety Alert for ACUSON SC2000 ultrasound systems, model 10433816, software version between VA16A and VA30A and Stress Eco option
Recall Or Safety Alert for Voyant Open Fusion clamp model EB40, lots: 1243964, 1243975, 1244125.
Recall Or Safety Alert for Thyroglobulin reagent kit for Access, reference 33860
Recall Or Safety Alert for Hemodialyzer SUREFLUX 25UX LC GA, lots 15B23F, 15D27F and 14L29F, 14I29F
Recall Or Safety Alert for Femoral components of the knee system AGC Dual Articular 2000
Recall Or Safety Alert for BEP Systems 2000 / BEP 2000
Recall Or Safety Alert for Puritan Bennett ™ 980 respirator, universal and neonatal models
Recall Or Safety Alert for Dimension Vista® Systems and Dimension® Clinical Chemistry Systems
Recall Or Safety Alert for Reusable blades of GlideScope GVL and AVL videolaringoscopes
Recall Or Safety Alert for Culture media "BBL ™ CHROMagar ™ MRSA II"
Recall Or Safety Alert for Coombs reactive Antiserum "Anti Jka (JK1)", reference 808176, lot 2409030-00
Recall Or Safety Alert for Artery catheters "PiCCO", Ref. PV2014L08-A, lot 15AF12 and Ref. PV2014L50-A, lot 15AG12
Recall Or Safety Alert for Digital radiography systems "DX-D100" type 5410 and "DX-D 100" Wireless type 5411
Recall Or Safety Alert for Femoral components of the revolving knee system "RHK"
Recall Or Safety Alert for Water traps "D-Fend", part number 876446-HEL, lot numbers, J9964985, J10201698, J10258248, J10284871, J10284872, J10344108 and "D-Fend +", order number 881319-HEL, lot numbers J9906966, J9965152, J10258251, J10300071
Recall Or Safety Alert for Ultrasound systems "ACUSON S Family" models 10041461, 10441701 and 10441730.
Recall Or Safety Alert for Reagent BD CD56 PE-Cy ™ 7, reference 335826, lots 4300715 and 4353883
Recall Or Safety Alert for Specimen cup containers of certain IMMULITE® / IMMULITE® 1000 Systems and in the micromesh tubes of the IMMULITE® 2000 / IMMULITE® 2000 XPi systems
Recall Or Safety Alert for rHead, uHead systems, trochial notch, ReMotion, Radius and Humerus Head
Recall Or Safety Alert for RaySearch RayStation 4.7.
Recall Or Safety Alert for SureFlex ™ Reusable Fibers and Separator and Segment Accessories for SureFlex ™ Reusable Fibers and Aura Reusable Fibers
Recall Or Safety Alert for Monal T60 and Monnal T60 JP fans
Recall Or Safety Alert for Open and closed screws "Polaris 4.75 Multi-Axial
Recall Or Safety Alert for OxiMax N-65 hand pulse oximeters, references N65-1 and N65P-1, and OxiMax N-560 desktop pulse oximeters, reference N560
Recall Or Safety Alert for Brainlab cranial navigation system
Recall Or Safety Alert for Lumbar Legras used in the implantation of intervertebral fusion boxes EIT Cellular Titanium®
Recall Or Safety Alert for Lot 96149 of the Zirconia Dental Abutment Rescue Instrument RP RP / WP, ref. 37882
Recall Or Safety Alert for Tests ALT, AST, CK-MB, GLDH, NH3
Recall Or Safety Alert for Therapy devices with ASV
Recall Or Safety Alert for "Twin rotary connector SHER-I-SWIV / FO", "Sher-I-Bronch left", "Sher-I-Bronch right" and "Accessory package for Sher-I-Bronch" of the "Endotracheal tube Hudson RCI® SHERIDAN SHER-IBRONCH ® "
Recall Or Safety Alert for Test "B · H · A · H · M · S PCT Direct", reference 126.025, lots 525699, 577857, 595599, 623573 and 643864
Recall Or Safety Alert for Radiation therapy planning systems RayStation 4.7, with software version 4.7.1.
Recall Or Safety Alert for CentraLink IT System, v14.0.5 and v14.0.8
Recall Or Safety Alert for ADVIA Centaur Tnl Ultra test
Recall Or Safety Alert for Reagent CK-NAC liqui UV, reference 12015, lots 14011, 14012
Recall Or Safety Alert for intracranial pressure monitoring catheters Road with Licox bolt IMC
Recall Or Safety Alert for Laboratory Automation Systems enGen ™
Recall Or Safety Alert for Laboratory Automation Systems enGen ™
Recall Or Safety Alert for Radiology systems D2RS, DX-D800 and XCELLENCE DYNAMIC
Recall Or Safety Alert for Optilite analyzers
Recall Or Safety Alert for Italian Cypress Allergen, material number 10386079, lots 206 and 208
Recall Or Safety Alert for Tagged of 4.0 mm Pedicle Puncture and Surgical Techniques Pangea Vertebral System, USS II Polyaxial, MATRIX: Deforming Disorders and Degenerative Disorders
Recall Or Safety Alert for MML valves
Recall Or Safety Alert for Oximetry modules of uSpO2 and HPLP, component number 1075383 of Philips Respironics USA
Recall Or Safety Alert for Reactive strips for the CIDEX OPA solution
Recall Or Safety Alert for X-ray system "DuraDiagnost 3.0 / 4.0", reference 712211, with configuration ES6600229514
Recall Or Safety Alert for Femoral knee implant, ref. 185285, lot 3422674, of the Vanguard Knee Revision System SSK 360 / DA360
Recall Or Safety Alert for FX dialysers CorDiax high permeability and Hemofiltros FX CorDiax
Recall Or Safety Alert for Dimension Vista® 500 intelligent laboratory system and Dimension Vista® 1500 intelligent laboratory system, using software versions 3.6.1, 3.6.1_MU3p and 3.6.1SP1
Recall Or Safety Alert for Constrained Insert R3 52 mm, order number 71339152, Item 14HM08235
Recall Or Safety Alert for Standard and lateralized Optimized stems
Recall Or Safety Alert for InstaTrak® 3500 Plus computer assisted navigation systems, ENTrakTM Plus, InstaTrak® 3500 and ENTrakTM
Recall Or Safety Alert for "Ysio Max", "Luminos dRF Max", "Luminos Agile Max" and "Uroskop Omnia Max" with the software version "VE10E"
Recall Or Safety Alert for Palindrome ™ catheter kit for long-term vascular access SI, HSI and HSI Precision
Recall Or Safety Alert for Kit 11-Desoxicortisol-RIA-CT, reference number KIPI20000
Recall Or Safety Alert for ultrasound systems "EPIQ 5", "EPIQ 7", "AFFINITY 50" and "AFFINITY 70" that do not include the option of Pediatric Cardiology
Recall Or Safety Alert for V-Sign ™ Sensors 2 of the SenTec Digital Monitoring System
Recall Or Safety Alert for Aurino L50 Exam Lamp
Recall Or Safety Alert for Lot 257 of the IMMULITE® / IMMULITE® 1000 kit Thyroxine transport globulin (LKTB1)
Recall Or Safety Alert for ORTHO VISIONTM analyzer for ORTHO BIOVUE® cassettes, catalog 6904579, software version 1.0.4
Recall Or Safety Alert for ORTHO VISIONTM analyzer for ORTHO BIOVUE® cassettes, catalog 6904579, software version 1.0.4
Recall Or Safety Alert for ultrasound systems "EPIQ 5", "EPIQ 7", "AFFINITY 50" and "AFFINITY 70" with the option of pediatric cardiology
Recall Or Safety Alert for The 1st generation CODMAN® CERTAS ™ Therapy Management System (TMS), Product Codes 82-8850 and 82-8850D
Recall Or Safety Alert for Dimension Vista® Thyroid stimulating hormone (TSH) LOCI® "
Recall Or Safety Alert for "Infusomat Space Line, TRANSP, UV-PROT, PUR, LL, 250 cm" and "Infusomat Space Line, Y-PORT, UV-PROT, PUR, LL, 250 cm"
Recall Or Safety Alert for GE Healthcare Magnetic Resonance Systems
Recall Or Safety Alert for TIGERPAW System II
Recall Or Safety Alert for BCS and BCS XP coagulation analyzers
Recall Or Safety Alert for Implantable Pulse Generator (GPI) "EonTM", Model 65-3716 for spinal cord stimulation, EonTM Model 3701 wall charger, EonTM Model 3711 portable charger and accessories
Recall Or Safety Alert for Needles AMICA PROBE
Recall Or Safety Alert for Advanced quantization software QLAB, version 10.0 of the Xcelera system with a2DQ and aCMQ applications
Recall Or Safety Alert for "SynchroMed® II" implantable drug infusion pumps, models 8637-20 and 8637-40, manufactured between December 5, 2014 and February 10, 2015, with certain serial numbers
Recall Or Safety Alert for Flex® Dimension Vista® Reagent Cartridge Phenytoin, catalog number K4064 SMN 10445125, lot numbers: 14163AB, and 14181AC
Recall Or Safety Alert for Laboratory Automation System enGen ™ with Select v5.0, Custom or Select v3.2.2 and earlier versions
Recall Or Safety Alert for Bimanual Ophthalmic Irrigation / Aspiration Cannulas Steriseal (Bi-Manual Irrigating / Aspirating Handpieces)
Recall Or Safety Alert for Blue test lung (blue test bag)
Recall Or Safety Alert for Certain batches of the Core Bard® Monopty® Biopsy Disposable Instrument
Recall Or Safety Alert for RAPIDPoint® 405 blood gas analyzer
Recall Or Safety Alert for X-ray digital angiographic systems Artis Q and Artis Q zen
Recall Or Safety Alert for PrimusRS rehabilitation system, PRRS model
Recall Or Safety Alert for Morpheus ™ Smart PICC CT
Recall Or Safety Alert for System covers used with the da Vinci Standard, S and Si Surgical Systems.
Recall Or Safety Alert for "Trellis 8 peripheral infusion system", references EVT808015, EVT808025, EVT812015, EVT812025, EUT808015, EUT808030, EUT812015 and EUT812030
Recall Or Safety Alert for Pressure regulators used with the Evicel® fibrin sealant.
Recall Or Safety Alert for Ball dilatation catheter for ATP ConQuest by Bard®,
Recall Or Safety Alert for Ultrasonic Cleaning Systems Cavowave Pro
Recall Or Safety Alert for AQT90 FLEX
Recall Or Safety Alert for AQT90 FLEX
Recall Or Safety Alert for Expel ™ drainage catheter
Recall Or Safety Alert for Instruments of the Autostainer staining systems
Recall Or Safety Alert for Bead Block ™ (embolizing microsphere)
Recall Or Safety Alert for Distal Triathlon Modular Capture Templates, reference 6541-1-723
Recall Or Safety Alert for fans "Engstrom Carestation and Engstrom Pro
Recall Or Safety Alert for Artificial respirator "Fabian HFO", model 7200
Recall Or Safety Alert for FORUM Viewer 3.1 and 3.2
Recall Or Safety Alert for wheelchairs Breezy PariX²
Recall Or Safety Alert for Reagents PF4 Concentrated Wash
Recall Or Safety Alert for Access 2 stand-alone integrated systems that include the Access 2 immunoassay systems and the Access UniCel DxC 600i Synchron system
Recall Or Safety Alert for of certain products ALLSET + ™ GOLD DRB1-13 HIGH RES and DRB1-13 SSP UNITRAY
Recall Or Safety Alert for Harmonic ACE instruments
Recall Or Safety Alert for Pediatric defibrillation electrodes, for Schiller defibrillators.
Recall Or Safety Alert for Cardiovascular interventional system Allura Xper FD10
Recall Or Safety Alert for Neonatal and pediatric defibrillation electrodes for the Corpuls defibrillators.
Recall Or Safety Alert for Zenith Alpha ™ Thoracic Vascular Endoprosthesis
Recall Or Safety Alert for Counterpulsation console with intra-aortic balloon (BCIA) CARDIOSAVE® Hybrid, references: 0998-00-0800-XX and 0998-UC-0800-XX (excluding 0998-00-0800-83)
Recall Or Safety Alert for Typing test of LABType HD DRB1, catalog identifier RSSOH2B1, lot number 009 and lot number 1-16.
Recall Or Safety Alert for Implantable Pulse Generator (GPI) "BrioTM", Model 65-6788 for deep brain stimulation, BrioTM Model 6721 Loader and BrioTM Model 3767 Loader Accessory
Recall Or Safety Alert for Edwards Commander Release System, Models 9610TF23, 9610TF26, 9610TF29
Recall Or Safety Alert for Edwards Commander Release System, Models 9610TF23, 9610TF26, 9610TF29
Recall Or Safety Alert for Juvederm Ultra4® intradermal filling implant
Recall Or Safety Alert for Sperm Test HBA, Reference 1132-002
Recall Or Safety Alert for Reagent IRON TPTZ liquicolor, reference 12290600, lots 13007, 13008, 13009, 13010, 14001, 14002, 14003
Recall Or Safety Alert for Bending and cutting pliers with pick, for LOCK 2.0 plates, reference 329.143
Recall Or Safety Alert for Phototherapy systems with NeoBLUE 2 LED panel kit
Recall Or Safety Alert for Pediatric defibrillation electrodes
Recall Or Safety Alert for Pediatric defibrillation electrodes
Recall Or Safety Alert for Single lumen ventilation circuits for Pneupac® respirators, with PEEP valve
Recall Or Safety Alert for Dialysis systems Artis / Evosys
Recall Or Safety Alert for Enzymatic creatinine, Cholesterol, Uric Acid, Lactate and Lipase
Recall Or Safety Alert for Direct X-ray system Dx-D 600 with semiautomatic configuration
Recall Or Safety Alert for Plugs for the syringes Luer, Yellow, and Luer Lock, Green, in DISCPAC container
Recall Or Safety Alert for Suspensions to the roof SA, manufactured between March 2012 and July 2014, of the surgical lighting systems of roof "PowerLED", "Hled", "Xten", "Standop Volista", "Hanaulux 3000"
Recall Or Safety Alert for Peripheral infusion system Trellis 8
Recall Or Safety Alert for Systems "Philips Monitoring Center IntelliVue Information Center (PIIC) iX
Recall Or Safety Alert for ARTIS / EVOSYS Dialysis Systems equipped with software 8.09.12, 8.09.13, 8.15.06 and 8.33.02
Recall Or Safety Alert for Antibacterial / Viral filters, heat / moisture exchanger (HME)
Recall Or Safety Alert for "Novocastra ™ Mouse Monoclonal Liquid Antibody", Product Code NCL-L-CD15
Recall Or Safety Alert for Puritan Bennett ™ 980 respirator
Recall Or Safety Alert for Puritan Bennett ™ 980 respirator
Recall Or Safety Alert for Implantable cardioverter defibrillators with radiofrequency capability: ELLIPSE, FORTY ASSURA, UNIFY ASSURA, and QUADRA ASSURA and pacemakers: ASSURITY AND ALLURE when used with the MERLÍN @HOME remote monitoring EX1150 RF transmitter
Recall Or Safety Alert for Brilliance CT Big Bore Systems, Ingenuity Core, Ingenuity Core128 and Ingenuity Flex
Recall Or Safety Alert for iPLAN RT / iPLAN RT Dose
Recall Or Safety Alert for IMMULITE / IMMULITE 1000 Androstenedione and IMMULITE 2000 / IMMULITE 2000 XPi Androstenedione Assays
Recall Or Safety Alert for IMMULITE / IMMULITE 1000 Androstenedione and IMMULITE 2000 / IMMULITE 2000 XPi Androstenedione Assays
Recall Or Safety Alert for Infusion equipment Comfort ™, Comfort ™ Short and Contact ™ Detach
Recall Or Safety Alert for Infusion sets Accu-Chek® TenderLink
Recall Or Safety Alert for Neonatal and pediatric defibrillation electrodes for the defibrillators Corpuls
Recall Or Safety Alert for Defibrillator for cardiac resynchronization therapy AUTOGEN CRT-D and implantable automatic defibrillator AUTOGEN ™ ICD DR
Recall Or Safety Alert for CyberKnife® Robotic Radiosurgery System with first-generation Iris ™ variable aperture collimator
Recall Or Safety Alert for Esprit V1000 fan, serial number VS3004712
Recall Or Safety Alert for Ultrasound systems EPIQ 5 and EPIQ 7, with software versions 1.0.x and 1.1.x, with the applications of a2DQ (Automatic Quantification of 2D Images) and aCMQ (Automatic Quantification of Cardiac Motility)
Recall Or Safety Alert for Bronchial Tubes, Bronchial Tubing Set and Tracheopart Set
Recall Or Safety Alert for IntelliSpace Portal and IntelliSpace Portal IX System, with software versions 6.0.0, 6.0.1, 6.0.2 and 6.0.3.
Recall Or Safety Alert for "Dimension Vista® 500 intelligent laboratory system" and "Dimension Vista® 1500 intelligent laboratory system"
Recall Or Safety Alert for VITROS® 3600 Immunodiagnostic Systems, product code 6802783 and VITROS® 5600 Integrated Systems
Recall Or Safety Alert for Clinical information systems Philips IntelliVue Clinical Information Portfolio (ICIP) and IntelliSpace Critical Care & Anesthesia (ICCA)
Recall Or Safety Alert for System 1 Advanced Perfusion System, reference 801764
Recall Or Safety Alert for Surgical Technique for the Zimmer Knee System Person, Article number 97-5026-001-00.
Recall Or Safety Alert for Accu2i pMTA Applicator, references 945900-600, 945900-601 and 945900-602
Recall Or Safety Alert for QIAamp DSP Virus Kit, reference 60704
Recall Or Safety Alert for TESS humeral inverted dome, TESS inverted humeral monobloc stem and associated TESS humeral inserts.
Recall Or Safety Alert for Affixus nail for hip fractures
Recall Or Safety Alert for FluoroType® HSV kit analyzer VER 1.0
Recall Or Safety Alert for Various DLP products
Recall Or Safety Alert for HCG pregnancy test and LH ovulation test for self-diagnosis.
Recall Or Safety Alert for FALSE CE MARKING IN SANITARY PRODUCTS
Recall Or Safety Alert for Consoles of intra-aortic counterpulsation (BCIA), distributed between 03-25-2003 and 11-12-2013: CS100i BCIA, reference 0998-UC-0446HXX; 0998-UC-0479HXX, CS100 BCIA, reference 0998-00-3013-XX; 0998-UC-3013-XX, CS300 BCIA, reference 0998-00-3.
Recall Or Safety Alert for Centricity Critical Care (CCC, formerly called Clinisoft) Version 7.0 2D service pack to 9.0
Recall Or Safety Alert for Brennen® 4.5 "mallador, references 131500, 131501, 131502, 131503, 131504 and 131506
Recall Or Safety Alert for Encore ™ inflation device 26. Unit package
Recall Or Safety Alert for Calibrator 30 for the enhanced ADVIA Centaur estradiol (eE2) test in the ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur XPT systems
Recall Or Safety Alert for Emergency cabinet MAVO 02 (F) AIR (B) ARICA, Reference 924462.
Recall Or Safety Alert for Sharesource Claria connection platform, product code 5CGM01, for use with the DPA system Homechoice Claria
Recall Or Safety Alert for Stryker SmartLife aseptic casing, large size, catalog no. 7126-120-000
Recall Or Safety Alert for Various traumatology and limb instruments (drills and dies)
Recall Or Safety Alert for Slides of PHYT VITROS® Chemistry Products (10758750004690), product code 8298671
Recall Or Safety Alert for Artis, X-Workplace, Sensis and Arcadis systems
Recall Or Safety Alert for COMPASS systems versions 3.1 and 3.1.4.0
Recall Or Safety Alert for Reagent cartridges Dimension® Theophylline (THEO) Flex
Recall Or Safety Alert for Synthetic suture monofilament, sterile DAFILON BLUE 2/0 (3) 75 CM DS 24, Reference C0935360
Recall Or Safety Alert for VICRYL ™ mesh bag by ETHICON
Recall Or Safety Alert for ADVIA Centaur and ADVIA Centaur XP Immunoassay Systems
Recall Or Safety Alert for Patient Monitors ItelliVue
Recall Or Safety Alert for "DG5000 Monitors-Defibrillators"
Recall Or Safety Alert for interlocking units Medi Clutch Lock and Medi Modular Clutch Lock
Recall Or Safety Alert for MultiDiagnost Eleva Systems with Flat Detector
Recall Or Safety Alert for Leksell Gamma Knife® Perfexion ™ equipment
Recall Or Safety Alert for ADVIA Centaur / Centaur XP systems
Recall Or Safety Alert for Vacuum systems Off-Pump ACROBAT V and ACROBAT SUV and Access devices AXIUS XPOSE 3 and AXIUS XPOSE 4
Recall Or Safety Alert for External drainage systems of LCR EDS 3 ™
Recall Or Safety Alert for CALCIBON 5G and 10G.
Recall Or Safety Alert for Stationary x-ray systems of digital angiography "Artis Zee and Artis Zeego" with software versions VC14 and VC21
Recall Or Safety Alert for Reagent ARCHITECH Total T3, Lots 38901UI00 and 38901UI01
Recall Or Safety Alert for COGNIS CRT-D, TELIGEN DR ICD and TELIGEN VR ICD
Recall Or Safety Alert for "Sunlift Steel Cranes", References G150 and G175
Recall Or Safety Alert for mammography systems Inspiration Mammomat
Recall Or Safety Alert for Puritan Bennett ™ 840 Respirator, References 4-840220DIEC-SP and 10019984
Recall Or Safety Alert for Battery of the Surgical Systems da Vinci S, Si and Si-e ", catalog number 371268-02.
Recall Or Safety Alert for vascular prostheses, bioprosthetic ducts and Thoraflex ™ Hybrid stent
Recall Or Safety Alert for AUTOFIX ™ 3.0 / 4.0 screws
Recall Or Safety Alert for Vascular thoracic endoprostheses Relay Plus and Relay NBS Plus
Recall Or Safety Alert for ACUSON SC2000 ™ ultrasound systems, software version 3.5
Recall Or Safety Alert for Camera systems Symbia T Series and Symbia Intevo
Recall Or Safety Alert for Transesophageal transducer V5Ms, models 8263703 and 8264577
Recall Or Safety Alert for Direct X-ray System Dx-D 600
Recall Or Safety Alert for IntelliSpace Portal System
Recall Or Safety Alert for IntelliSpace Portal System
Recall Or Safety Alert for IntelliSpace PACS System, Software Version 4.4., With the "Auto Export" option enabled
Recall Or Safety Alert for Reagent Cartridge Flex® Hemoglobin A1c (HbA1c)
Recall Or Safety Alert for FlexLab Automation Modules with antennas controlled by the MOL-A electronic card
Recall Or Safety Alert for Rotating hinge S-ROM Noiles for femur with pin
Recall Or Safety Alert for Implantable Automatic Defibrillators (ICDs) EllipseTM
Recall Or Safety Alert for Trays ProcedurePack®
Recall Or Safety Alert for inks and tattoo needles
Recall Or Safety Alert for Software card model 8870
Recall Or Safety Alert for CA 19-9 reagent pack from VITROS® and CA 19-9 Calibrators from VITROS® Immunodiagnostic Products
Recall Or Safety Alert for Advanced quantification software QLAB, versions 10.0 (Reference 61704771) and 10.1 (Reference 61728001)
Recall Or Safety Alert for Semiautomatic defibrillator / pacemaker with modular multiparameter monitor corpuls3
Recall Or Safety Alert for Integrated Systems of Clinical Chemistry Dimension EXL 200, LM, STM, catalog numbers 10636928, 10472176 and 10639338
Recall Or Safety Alert for TheraSorb TPE LIFE 18 Tubing Set
Recall Or Safety Alert for intra-aortic counterpulsation consoles (IABP) Datascope System 98 / 98XT, CS100® / CS100i and CS300 ™
Recall Or Safety Alert for intra-aortic counterpulsation consoles (IABP) Datascope System 98 / 98XT, CS100® / CS100i and CS300 ™
Recall Or Safety Alert for CARESCAPETM B650 monitors with software versions included 1.1.12.26 or earlier
Recall Or Safety Alert for Precision 500D and Proteus XR / a devices, equipped with the Wireless Digital Radiography System (WDR1), software version V13 and V14
Recall Or Safety Alert for "Astrada intrathecal catheter with 86 cm intraspinal segment" (model 8780), "Ascenda intrathecal catheter with 66 cm intraspinal segment" (model 8781) and "Ascenda revision kit" (model 8784)
Recall Or Safety Alert for Version 01 of the Neuromuscular Transmission Module (E-NMT-01)
Recall Or Safety Alert for Expansion catheter for ACTP RX NC Cordis EMPIRA ™ (75RxxyyyN) and Dilatation catheter for ACTP RX Cordis EMPIRA ™ (85RxxyyyS)
Recall Or Safety Alert for Digital radiography system DX-D 100
Recall Or Safety Alert for CARESCAPETM monitor B850, B650 or B450 with software versions between 2 and 2.0.4
Recall Or Safety Alert for Manual switch of the CT Exprès ™ 3D contrast injection system
Recall Or Safety Alert for Mobile radiography units Digital DX-D 100
Recall Or Safety Alert for Amulet digital mammography system
Recall Or Safety Alert for Lots 23366, 23882, 24228, 24963 of the ready-to-use Primary Antibody Bond ™ Thyroglobulin (1D4), product code PA0025
Recall Or Safety Alert for Directional arm for distal femoral nail, reference 357.136, lot number 2134270
Recall Or Safety Alert for Fixed Backup, reference 1555323, lot numbers 13GXB0001 and 13IXB0001
Recall Or Safety Alert for Puritan Bennett ™ 840 respirator, with 9.4-inch graphical user interface (GUI). References 4-840220DIEC-SP and 4-076030-00
Recall Or Safety Alert for Puritan Bennett ™ 840 Respirator, References 4-840220DIEC-SP
Recall Or Safety Alert for Prostatic catheter lined with hydrogel 3-way straight tip
Recall Or Safety Alert for NAV3i Navigation Systems
Recall Or Safety Alert for Needles for USB and USC Ultrasound
Recall Or Safety Alert for Gasometric Analyzers RAPIDPoint® 500 Series
Recall Or Safety Alert for OASYS Magnetic Resonance Systems, models M701, M704, M706 and M711
Recall Or Safety Alert for Digital angiographic systems Axiom Artis or Artis zee in connection with the manual switch with order number 3771750 used in the patient table to acquire an X-ray image
Recall Or Safety Alert for Control N of the Anti- T. pallidum of the "Enzygnost® Syphilis Assay"
Recall Or Safety Alert for System syngo RT Dosimetrist virtual simulation software version 2.7.29
Recall Or Safety Alert for Vivid E9 Ultrasound Equipment with software versions 113.0.1-113.0.5 and Probes C1-5-D, C2-9-D, IC5-9-DY M5Sc-D
Recall Or Safety Alert for Haemostatic Endoscopic Device Hemospray, References HEMO-7-EU and HEMO-10-EU
Recall Or Safety Alert for Radiation therapy treatment planning systems RayStation with software version 4.0.3.4
Recall Or Safety Alert for Immunochemistry Systems • MODULAR ANALYTICS <E170> ref. 03617505001 • MODULAR ANALYTICS EVO <E170> ref. 04998642001 • Module cobas e 601 ref.04745922001 • Module cobas e 602 ref. 05990378001
Recall Or Safety Alert for IntelliSpace Systems Critical Care and Anesthesia and IntelliVue Clinical Information Portfolio
Recall Or Safety Alert for ECHELON Flex 60 articulated linear endocutter, EC60A product code and "Laparoscopic Sleeve Resection Pack" gastrectomy kit, references LSR30 and LSR31
Recall Or Safety Alert for Ventricular catheter
Recall Or Safety Alert for Ysio Systems
Recall Or Safety Alert for ADAC Systems Vertex Classic, Vertex Plus, Solus and Vertex V60
Recall Or Safety Alert for Tension band nails Acumed (Acumed Tension Band Pin)
Recall Or Safety Alert for MGuard Prime Coronary Stent Systems EPS-Stent against embolisms
Recall Or Safety Alert for 50 cm and 90 cm implant AXIUM® derivation set
Recall Or Safety Alert for Medstream® programmable infusion pumps
Recall Or Safety Alert for A200 and Skippi electronic wheelchairs
Recall Or Safety Alert for Bard® Ventralight ™ ST Mesh with PS Echo PS ™ and Bard® PS Positioning System Composix ™ L / P Mesh with Echo PS ™ Positioning System
Recall Or Safety Alert for Guiding Needle 3.2 mm in diameter and 400 mm in length, reference no. 357.399
Recall Or Safety Alert for Guiding Needle 3.2 mm in diameter and 400 mm in length, reference no. 357.399
Recall Or Safety Alert for X-ray digital angiographic systems AXIOM Artis, Artis Zee or Artis Q "with a wireless footswitch
Recall Or Safety Alert for FUJIFILM AMULET digital mammography system, models FDR-1000AWS, FDR-2000AWS, FDR-3000AWS, software versions V5.1.0001-0007, with biopsy unit
Recall Or Safety Alert for Laboratory Automation Systems enGen ™ (enGen ™ Systems) with TCAutomation (TCA) software v.2.6, v3.2 and v3.5 and configured with Bypass Module for the ADVIA Centaur®, Abbott Architect ™, VITROS® and / or Tosoh AIA
Recall Or Safety Alert for Cavafix and Drucafix catheters
Recall Or Safety Alert for Syngo Workflow radiology system used in Portal Radiologist
Recall Or Safety Alert for Monnal T40 and T50 fans
Recall Or Safety Alert for Stainless Steel Monofilament Suture and Polygonic Acid Suture Bondek Plus
Recall Or Safety Alert for Innovative cardiovascular radiology systems, models 2100IQ, 2121IQ, 3100, 3100IQ, 3131IQ, 4100, 4100IQ, IGS 620 and IGS 630, equipped with PDB (junction box)
Recall Or Safety Alert for Reagent FB (Fast Blue BB), Ref .: 70562 and Reagent ZYM B, Ref .: 70493. These reagents are also included in API Listeria products, Ref .: 10300, and API NH, Ref .: 10400.
Recall Or Safety Alert for WECK® Vista ™ laparoscopic access cannulas and ports
Recall Or Safety Alert for Blood Lines for Unipuncture for AK machines
Recall Or Safety Alert for Presser for ODALYS screws, ref. SD0100
Recall Or Safety Alert for Sysmex automatic coagulation analyzer, model numbers CS-2000i, CS-2100i and CS-5100, used in conjunction with the Chromogenic FVIII reagent (B-4238)
Recall Or Safety Alert for ACUSON P300TM ultrasonic imaging system, when used with the PA230 transducer
Recall Or Safety Alert for NMARQ ™ circular and growing irrigated catheters, catalog numbers D132214 and D132215 and nMARQTM multi-channel radio frequency generator
Recall Or Safety Alert for Actim CRP tests. Lots: 0030416, 0030253, 0030142, 0030015, 0029746, 0029745, 0029435, 0029150, 0029148
Recall Or Safety Alert for Sengstaken and Endoguía RUSCH probe
Recall Or Safety Alert for Base Station for recharging GemStar infusion pumps
Recall Or Safety Alert for Total T4 Calibrators of VITROS® Immunodiagnostic Products and Total T4 Reagents of VITROS® Immunodiagnostic Products
Recall Or Safety Alert for Rusch Bronchopart®, Rusch Bronchopart® white, Bronchial tube of a lumen Rusch right and Rusch Tracheopart® "
Recall Or Safety Alert for Lot 1265366 of the product Oxoid Reagent Legionella pneumophilia serogroup 2-14
Recall Or Safety Alert for Calibrator BRAHMS Free βhCG Kryptor CAL, kit number reference 80991, lot 09045
Recall Or Safety Alert for MINISEND Luer Lock plugs, TP references, TP-INTER
Recall Or Safety Alert for Micro-Tech Spiked Biopsy Forceps
Recall Or Safety Alert for Alere Triage® TOX Drug Screen, catalog number 94400EU
Recall Or Safety Alert for Surgical Technique, Handle and Blades for Preparation of the Cadisc® 2G Endplate - C
Recall Or Safety Alert for Lenus Pro® Implantable Infusion Pumps
Recall Or Safety Alert for Cortical screw diameter 3.5 mm, length 12 mm, pure titanium, model number 404.012, lot number 3008521
Recall Or Safety Alert for "PRONTOPRIME with Emoluer valve"
Recall Or Safety Alert for Activa® PC, Activa® PC + S, Activa® RC, Activa® SC, all Restore® devices (including SureScan®), PrimeADVANCED®, PrimeADVANCED® SureScan® MRI and Itrel® 4
Recall Or Safety Alert for Chemistry Systems ADVIA 1800 and 2400 with ISE firmware V2.23,
Recall Or Safety Alert for Arrow® Edge® Extended Access Hemodialysis Catheter Sets and Arrow® NextStep® Extended Access Antegrade Insertion Hemodialysis Catheter Sets
Recall Or Safety Alert for "Sunlift Cranes", Micro Model, batch number from MICR13094665 to MICR14014798
Recall Or Safety Alert for F5-01 portamódulos of the CARESCAPE ™ B850 Monitor
Recall Or Safety Alert for ELS syringes 200 ml and ELS syringe sets, references 316025, 316026, 317616, 317624, 317625, 317627 and 317628
Recall Or Safety Alert for Reference Electrode, Catalog Number 03111873180, used with the Systems: OMNI C, Cobas b 121 and cobas b 121 <BGE> , OMNI S and cobas b 221.
Recall Or Safety Alert for Certain heat exchangers for cardioplegia PLEGIOX
Recall Or Safety Alert for Sampling devices PerkinElmer 226, lot 412401
Recall Or Safety Alert for MINISEND Luer Lock plugs, TP references, TP-INTER, TP-MF, TP-MF-A, TP-F, TP-LUER-E
Recall Or Safety Alert for Family of Infusion Pumps PLUM LifeCare ™ 5000 and PLUM XL ™
Recall Or Safety Alert for Buckets for activated partial thromboplastin time (APTT) with citrate, catalog number J103C
Recall Or Safety Alert for "Segmental system polyethylene inserts Zimmer-sizes B and C", Models 00-5850-012-95 and 00-5850-013-95
Recall Or Safety Alert for Puritan Bennett ™ 840 and 700 Series (740 and 760) Respirator Oxygen Sensor
Recall Or Safety Alert for GemStar ™ Infusion Pumps, previous versions and including phase 3
Recall Or Safety Alert for GemStar ™ Infusion Pumps, previous versions and including phase 3
Recall Or Safety Alert for anesthesia devices Aisys CS2, Aisys, Advance CS2, Avance, Amingo, Aespire and Aestiva
Recall Or Safety Alert for Programs of the LabPro Systems RSM V4.11-A (SMN: 10803933) and LabPro Panel Update 5 Multiregional (MR), (SMN: 10805894)
Recall Or Safety Alert for Implantable low-profile access with Broviac catheter with a lumen of 6.6 Fr
Recall Or Safety Alert for Test kit BBL Staphyloslide ™ Latex ", Ref 240952, Lot 1298966,
Recall Or Safety Alert for Kit HER2 CISH PharmDx ™, catalog number SK109, batches 00092789 and 20002057
Recall Or Safety Alert for Torque wrench XIA, XIA 3, XIA Elegance Short, Mantis Redux, references 03807028, 48237028, 482397028, 48287028 and several lots
Recall Or Safety Alert for Lp (a) SPQ ™ II Reagent Set, part number 86084 and Lp (a) IgG Antibody Reagent, 10mL, part number 88530
Recall Or Safety Alert for Anti-HBs Calibrators and Reagents from Vitros® Immunodiagnostics Products Lot 2500 and above
Recall Or Safety Alert for Rechargeable lithium batteries (catalog number 46827), used in the Hospital Blood Glucose Measurement Systems Nova StatSrip and StatSensor
Recall Or Safety Alert for • Gemini TF 16 and Gemini TF 64 PET / TAC systems, software versions 3.5.1, 3.5.2 and 3.5.2.2 • TruFlight Select PET / TAC systems, software version 3.5.3
Recall Or Safety Alert for LIFE 18 ™ apheresis system
Recall Or Safety Alert for EnGen ™ Laboratory Automation Systems configured with the software Select Select v 5.0
Recall Or Safety Alert for Portex® Gasometry Syringes
Recall Or Safety Alert for Instructions for Use of the STERRAD® Enhancer ref. 15400-020 and STERRAD® Adapter ref. 15401, 15402, 15403 (LA-104421-0002 rev.A)
Recall Or Safety Alert for Digital linear accelerators of the PRIMUS ™, ONCOR ™ and ARTISTE ™ type
Recall Or Safety Alert for Base Station for recharging GemStar infusion pumps, catalog numbers 13075-XX-07 and 13075-XX-09
Recall Or Safety Alert for Eclipse ™ treatment planning systems, ARIA® for radiation oncology, ARIA® Radiation for radiation therapy management and Acuity ™
Recall Or Safety Alert for Puritan Bennett ™ 840 respirators, reference 4-070201-85
Recall Or Safety Alert for Biological indicator STERRAD CycleSure 24, Ref. 14324
Recall Or Safety Alert for Measuring Cartridges RAPIDPOINT® 500
Recall Or Safety Alert for AQURE system, version 1.5.4, reference 933-501
Recall Or Safety Alert for LIAISON®Biotrin Control Parvovirus B19 IgM
Recall Or Safety Alert for VitreaCore Software
Recall Or Safety Alert for Olympus miniETD2 PAA washer-disinfectors, manufactured since August 2013 and Olympus miniETD2 PAA and ETD3 PAA washer-disinfectors that have been replaced since August 2013 by the DOS3 pump
Recall Or Safety Alert for Bottles for culture BacT / ALERT® PF PLUS and BacT / ALERT® FA PLUS
Recall Or Safety Alert for CentraLink ™ data management computer system, software version 14.0.8, catalog number 10814877
Recall Or Safety Alert for Propaq LT vital signs monitor (Propaq 802) with Nellcor SP02, Models 802LTAN, 802LT0N and 802LTRN, affected serial numbers KA124186, KA25981 and from KA002129 to KA027191
Recall Or Safety Alert for Volumed infusion pumps "Volumed μVP7000 Premium", "Volumed μVP7000 Classic Plus", "Syramed μSP6000 Premium" and "Syramed μSP6000 Classic Plus",
Recall Or Safety Alert for Desktop Transformer (Power Unit) GemStar ™ Infusion Pump, 3V DC, Catalog No. 13072-92-05
Recall Or Safety Alert for AcrySof® CACHET® Phakic Lens, models L12500, L13000, L13500 and L14000
Recall Or Safety Alert for AcrySof® CACHET® Phakic Lens, models L12500, L13000, L13500 and L14000
Recall Or Safety Alert for AcrySof® CACHET® Phakic Lens, models L12500, L13000, L13500 and L14000
Recall Or Safety Alert for Sengstaken tubes and probes
Recall Or Safety Alert for Inzii Withdrawal System 12/15 mm, reference CD004
Recall Or Safety Alert for Anti-HBs Calibrators and Reagents from Vitros® Immunodiagnostics Products
Recall Or Safety Alert for "High level disinfectant solution NU-CIDEX®", Reference NCX010
Recall Or Safety Alert for "Transradial arterial access equipment"
Recall Or Safety Alert for Blood glucose meter Accu-Chek® Aviva Combo, model 680, Ref .: 0515193700X, serial number equal to or greater than 68010200001
Recall Or Safety Alert for Certain references and batches of the products "Cervical distractor, right, with adjustable angle", "Extraction instrument for T-PAL", "Toothed rod separator for Matrix" and "Implant inserter"
Recall Or Safety Alert for Discovery NM / CT670, Optima NM / CT640, Discovery NM630 and Brivo NM615 systems
Recall Or Safety Alert for Ratchet handles, reference 07.00438.001, included in the ALP Trinica instrument trays
Recall Or Safety Alert for UniCel Dxl Access 800 and 600 and Unicel DxC 880i, 860i, 680i and 660i Immunoassay Systems
Recall Or Safety Alert for Hemosil Synthasil Reagent
Recall Or Safety Alert for TomoFix plate for medial proximal tibia (MHT). Catalog numbers 440.834 (S) and 440.831 (S).
Recall Or Safety Alert for COULTER® GENS ™ Systems, Catalog Number 6605381
Recall Or Safety Alert for In vitro diagnostic chemiluminescence system UniCel DxC 600i
Recall Or Safety Alert for XN-10 and XN-20 configuration modules of the XN Series Hematology Analyzers
Recall Or Safety Alert for Resistance Loss Syringes with Luer Lock connection - BD Epilor ™ 7ml Luer-Lok ™ (LOR)
Recall Or Safety Alert for Dimension Vista® 500 Systems Ref .: 10488224 and Dimension Vista® 1500, Ref .: 10444802 with software versions 3.5.1 or earlier
Recall Or Safety Alert for Immunohistology Systems "Bond Polymer Refine Red Detection System", Ref .: DS9390, and "ChromoPlex 1 Dual Detection for BOND", Ref .: DS9477
Recall Or Safety Alert for RAPIDPoint® 400 Series, 500 Series and RAPIDLab® 1200 Series
Recall Or Safety Alert for AVEA fans
Recall Or Safety Alert for Software application card for the N'Vision medical programmer
Recall Or Safety Alert for Flat panel detector (FPD, Flat Panel Detector) of the BrightView XCT image system
Recall Or Safety Alert for External Fixation Systems for Synthes Traumatology (Ex-Fix Systems) small, medium, osteogenesis ring by distraction (OD) and large
Recall Or Safety Alert for OSOM C. difficile kit Toxin A / B, Reference 173E
Recall Or Safety Alert for Analysis software "CardiacVX" (1.1.0 Ext. D) and "CardiacVX Flow" (1.1.0 Ext. D) executed on the Advantage Workstation
Recall Or Safety Alert for Torque wrench XIA, XIA 3 and XIA Elegance cuts, references 03807028, 48237028 and 48239028, lot numbers 125710, 11E042, 11E044, 11E047, 11A957, 11E035, 11E036 and R11E036
Recall Or Safety Alert for Probe cap for trepanning with and without latex with gel,
Recall Or Safety Alert for 7 mm Endo-Model® metal base tibial plate, references 15-2030 / 01, 15-2030 / 05 and 15-2030 / 09, of the LINK® Unicondylar Prosthesis
Recall Or Safety Alert for Lp (a) SPQ ™ II Reagent Set reference 86084 and Lp (a) IgG Antibody Reagent, 10 ml reference 88530
Recall Or Safety Alert for EasyLink ™ Computer System, Ref .: 10444799, 10444800 and 10487219
Recall Or Safety Alert for EasyLink ™ Computer System, Ref .: 10444799, 10444800 and 10487219
Recall Or Safety Alert for IMMULITE / IMMULITE 1000 T3 free and IMMULITE2000 / IMMULITE 2000 XPi T3 free kits
Recall Or Safety Alert for Hematology Analyzers ADVIA® 2120 (SMN 10361162) and ADVIA® 2120i (SMN 10361798), connected to the ADVIA® Autoslide system (SMN 10282177)
Recall Or Safety Alert for Allura Xper FD10 Cardiovascular Intervention Systems with floor suspension and "biplane" systems Allura Xper FD10 / 10
Recall Or Safety Alert for All batches with No. 326119 or lower of the Antimullerian Hormone ELISA Kit (AMH) Gen II, reference A79765
Recall Or Safety Alert for Culture medium Agar XLD, reference number 43563, lot number 1002115760
Recall Or Safety Alert for ADVIA Centaur Folate Kit containing Folate ReadyPack® primary reagent cartridges with lot number 071218
Recall Or Safety Alert for Philips TAC models Brilliance 16 Water, Brilliance 10 Water, Brilliance 6 Water, MX8000 Quad, MX8000 Dual, MX8000 Dual EXP, MX8000IDT 16, MX8000IDT 10
Recall Or Safety Alert for Immunoassay systems: Access 2 Immunoassay Systems, UniCel DxI 800 Immunoassay Systems, UniCel DxI 600 Immunoassay Systems, and UniCel DxC 880i, 860i, 680i and 660i Integrated Systems
Recall Or Safety Alert for Free locking systems for Zimmer femoral fixation, VERSA-FX® femoral fixation systems and VERSA-FX® II femoral fixation systems
Recall Or Safety Alert for Axis-Shield RPR - FRPR500, lot 802892541, 802893530 and 802893607
Recall Or Safety Alert for CARESTREAM DRX-Evolution equipment with software version V5.5.410.33 MR2
Recall Or Safety Alert for VORTEK® open / open double loop ureteral stent with attachable pusher and VORTEK® dual-loop ureteral stent with included in its kit the CH / FR 4.8 / 75 cm attachable pusher.
Recall Or Safety Alert for Certain lots of the "Small Peripheral Cutting Balloon Monorail Microsurgical Dilation Device 4.00mm x 15mm"
Recall Or Safety Alert for Updates of software versions 3.20.00 or 3.30.00, coming from versions 3.10.00 or 3.20.00, in the "Radiation Therapy Planning Systems (RTP) Monaco"
Recall Or Safety Alert for ADVIA Centaur Homocysteine Kit (HCY), for use in ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur CP systems
Recall Or Safety Alert for Extension device 1150.59AC of the table Alphamaquet 1150
Recall Or Safety Alert for Certain batches of self-tapping stainless steel dynamic locking screws, "Stardrive® Ø 2.4 mm, length 12 mm" and "Stardrive® Ø 2.7 mm, length 12 mm"
Recall Or Safety Alert for Probe for prostatectomy PROSTAFLOW ™ PVC and latex 20 CH / FR, article number AB7220, lot 3600135
Recall Or Safety Alert for "Instruments for the insertion of plates. For osteosynthesis of minimally invasive plaques (MIPO) ", model 0X6.000.127
Recall Or Safety Alert for Bola Leyla articulation clamp, model R2383 Also included in the Leyla Assembly Accessories Chart, catalog number R2385.
Recall Or Safety Alert for Reagent Cartridge Flex® Dimension Vista® RF ", catalog no. K7068 Material no. Siemens 10445908, lot 12283MA
Recall Or Safety Alert for implants (femur, kneecap, joint surface) and provisional components NexGen® CR Micro
Recall Or Safety Alert for Reagent cartridge Dimension TACR Flex and its associated calibrator
Recall Or Safety Alert for Software version 6.2 in Spanish (SMN 10701346), of the ADVIA 120 system
Recall Or Safety Alert for Patient transport stretcher TRANSLIFE 4749.01A0
Recall Or Safety Alert for Digital accelerators with electrons and beam modulator (Beam Modulator), MLCi / MLCi2, Agility or Asymmetric Heads
Recall Or Safety Alert for GemStar infusion system
Recall Or Safety Alert for Reduction instrument for spondylolisthesis, standard, for Matrix 5.5, Component number 03.632.008
Recall Or Safety Alert for Astelion Computerized Tomography Scanner: TSX-032A and Aquilion models: TSX-101A, TSX-201A, TSX-301A, TSX-301C and TSX-303A models.
Recall Or Safety Alert for Data Measurement System (DMS) of SOMATOM Emotion equipment
Recall Or Safety Alert for 1.5T Body SENSE coils with 12NC identification code, references 4522 131 5575x, 4522 132 1985x, 4522 132 7619x, 4598 000 5187x, 4598 000 5189x and 4598 003 59051 (where "x" is a number from 1 to 9), used with Magnetic Resonance Systems
Recall Or Safety Alert for angiographic catheters Beacon® Tip
Recall Or Safety Alert for EnVeo ™ R Mounting System, Model: LS-EnVeoR-23 and LS-EnVeoR-2629
Recall Or Safety Alert for CAMLOG Screw line dental implant, reference K1042.4311, lot 0030054130
Recall Or Safety Alert for Getinge washer-disinfectors of the 86 series with G1 control system, models S-8666 and S-8668 and software version up to and including 1.5.1.
Recall Or Safety Alert for Instrumentation of the femorotibial joint surface ATTUNE INTUITION
Recall Or Safety Alert for Surgical Incision Blades Raucodrape Surgical 55X80 cm, ref. No. 25447, lot 444212206
Recall Or Safety Alert for Individual (2385123-2) and double (2385125-2) LCD monitors used with classic Precision 500D radiographic and fluoroscopic systems
Recall Or Safety Alert for 3M ™ ESPE ™ Lava ™ Ultimate CAD / CAM Restoratives
Recall Or Safety Alert for "Philips Efficia DFM100 Defibrillators / Monitors", model 866199
Recall Or Safety Alert for surgical tissue bags Lapsac
Recall Or Safety Alert for Modules of Normo-Hypothermia 1T and 3T, code 16-02-50, 16-02-80, 16-02-81, 16-02-82, 16-02-83, 16-02-85, 16-02- 95
Recall Or Safety Alert for Lot 62763724 of the femoral nail for the greater trochanter of the "Zimmer Natural Nail" system, right, 10 mm in diameter and 32 cm in length, reference number 47-2492-320-10
Recall Or Safety Alert for Radiographic and fluoroscopic systems "Precision 500D" and "Advantx Legacy / Legacy-D", serial numbers 24003791-32 and 2403791-40.
Recall Or Safety Alert for Canned dies Navigation
Recall Or Safety Alert for Anti-radiation screens and surgical lamps suspended from the ceiling, installed by GE Healthcare or its agents
Recall Or Safety Alert for Certain references and lots of the PSA (Prostate-Specific Antigen) test used in certain IMMULITE® systems
Recall Or Safety Alert for 6 'interconnect cable, catalog number 39E23R, lot numbers 15697131L and 15789072L
Recall Or Safety Alert for Sonopet consoles of 110 V, 100 V and 230 V, references 5450-850-000, 5450-851-000 and 5450-852-000
Recall Or Safety Alert for Olympus Irrigation Pump, model OFP-2, Ref .: K10001143, serial numbers 21301660, 21304006, 21304095 and 21305828
Recall Or Safety Alert for Monitor / Defibrillator HeartStart MRx, models M3535A and M3536A,
Recall Or Safety Alert for "Alaris® GP, GP Guardrails®, GP Plus and GP Plus Guardrails® infusion pumps", References 80263UN01, 80263UN01-G, 9002MED01, 9002MED01-G, manufactured between December 2009 and January 2012
Recall Or Safety Alert for Supports, material number SMN 10309266, of the optical cover of the hematology system ADVIA® 120
Recall Or Safety Alert for Infusers with rolled tube (portable elastomer infusion pump system)
Recall Or Safety Alert for Resorbable BioMend® and BioMend® Extend ™ Collagen Membranes, and Resorbable Collagen Dressings for CollaTape®, CollaCote® and CollaPlug® Mouth Surgery
Recall Or Safety Alert for Multi-sheet 3D dynamic line collimation systems DMLC IV, DMLC electronic controller MKV 81-3A
Recall Or Safety Alert for Certain screws for self-tapping dynamic cobalt-chrome alloy locking, sterile, "Stardrive® Ø 3.7 mm, length 22-70 mm,", and "Stardrive® Ø 5.0 mm, length 32-90 mm"
Recall Or Safety Alert for Disposable equipment and collector equipment for HomeChoice
Recall Or Safety Alert for Certain batches of the BD Plastipak 50ml Luer Lok Syringe - Sterile, Ref .: 300865
Recall Or Safety Alert for Da Vinci system model IS1200, Forceps bipolar Precise of 8mm, Forceps bipolar Maryland of 8mm, Forceps bipolar F of 8mm
Recall Or Safety Alert for Mini Arco in C FLUOROSCAN ™, InSight and InSight2 models, with software versions Insight: 1.x, 2.x, 3.x; InSight2: 4.0, 4.0.1, 4.0.2
Recall Or Safety Alert for Lot W18499722 of the Transradial Access Equipment with Spring RADIALSOURCE ™ Guide, catalog number 505615S
Recall Or Safety Alert for Mobile radiography units DX-D 100 with wireless detector and DX-D 100 with connected detector
Recall Or Safety Alert for ECHELON ™ 60 ENDOPATH® refill for Black 4,4 mm Linear endoscopic stapler and cutter, 6 rows, model ECR60T
Recall Or Safety Alert for Washing solution Dimension®, Ref .: RD701, lots RD23031, RD23111, RD23241, RD23311, RD23391 and RD23461
Recall Or Safety Alert for CODMAN® CERTAS ™ Programmable Valves
Recall Or Safety Alert for CMF Screws MatrixNEURO, CMF Screws MatrixMIDFACE, MANDIBLE, and ORTHOGNATHICS
Recall Or Safety Alert for Dimension Vista® 500 and Dimension Vista® 1500 analyzers, with software versions 3.4 and 3.5.1.
Recall Or Safety Alert for MMB Calibrator in Dimension® Clinical Chemistry Systems
Recall Or Safety Alert for NephroMaxTM balloon catheter for high-pressure nephrostomy and NephroMaxTM balloon catheter kit for high-pressure nephrostomy
Recall Or Safety Alert for Monitor / Defibrillator HeartStart MRx
Recall Or Safety Alert for Easypump® C-bloc ™ RA + Select-A-Flow ™ + OnDemand ™, Ref .: 4440008, lots: 152803, 182313 and 192472
Recall Or Safety Alert for BBL DrySlide ™ PYR Kit and BBL Dryslide ™ Oxidase kit
Recall Or Safety Alert for "Oxoid Antimicrobial Susceptibility Testing Disc CN10 (Gentamicin)"
Recall Or Safety Alert for "Oxoid Antimicrobial Susceptibility Testing Disc AMP10 (Ampicillin)"
Recall Or Safety Alert for X-ray Systems Imaging Volume (XVI) with software version 4.5.1
Recall Or Safety Alert for Infusion set Plum A + ™, ref .: 12193, 12194, 12195 and 12196
Recall Or Safety Alert for Kirschner needle diameter 2.6 mm with spatula tip, length 500 mm, sterile, model 292.001S
Recall Or Safety Alert for Clinical Chemistry Analyzers AU2700 / AU2700 Plus and AU5400, (Customers with complete MOD (modifications) AU2700-184 and AU-5400-190), manufactured between April 1999 and July 2012
Recall Or Safety Alert for TAC Brilliance CT 64, Ingenuity Core and Ingenuity Core 128 Systems
Recall Or Safety Alert for Battery modules reference 6487180, for use with the MAQUET SERVO-i ventilation systems, manufactured between 01 February 2010 and 25 October 2012 inclusive, date of manufacture code 1005 to 1243
Recall Or Safety Alert for Tests of Siemens ADVIA Centaur, Dimension, Dimension Vista and IMMULITE
Recall Or Safety Alert for MicroSTREP plus Type 1 panels
Recall Or Safety Alert for LifeCodes PF4 Enhanced Assay
Recall Or Safety Alert for Embryo transfer catheters Sure-Pro® and Sure-Pro Ultra®
Recall Or Safety Alert for DuraGen® Dural Graft Matrix collagen sponges, DuraGen Plus ™ Adhesion Barrier Matrix, DuraGen ™ Dural Regeneration Matrix Suture, Neurawrap® Nerve Protector and NeuraGen® Nerve Guide
Recall Or Safety Alert for Flexible Handles for cannulated sliding guide, for universal intramedullary nails (ref 355.220), catalog number 355.280, (old design), up to lot 5918663 inclusive
Recall Or Safety Alert for AQUARIUS Hemofiltration Devices, Ref. GE-F096-00
Recall Or Safety Alert for "Oxoid Antimicrobial Susceptibility Testing Disc ETP10 (Ertapenem)", model CT1761B, Lot 1227786
Recall Or Safety Alert for Elecsys β-CrossLaps serum test (β-CTx), reference 11972308-122, used in the Elecsys and Cobas immunoanalyzers e.
Recall Or Safety Alert for LOCK plate for tension band 2.0 right, profile molded, 4 holes, pure titanium, lots 5176395, 5470579, 5486366
Recall Or Safety Alert for Da Vinci Surgical System
Recall Or Safety Alert for Application Vitrea CT Brain Perfusion 2D, versions 6.0 and later for Vitrea Enterprise Suite, Vitrea, VitreaAdvanced, and Vitrea fX
Recall Or Safety Alert for Axes of Probe Plus II Electrosurgery Probes ENDOPATH®
Recall Or Safety Alert for Active Implantable Defibrillator (DAI) Fortify ST ™, models CD1235-40, CD1235-40Q, CD2235-40 and CD2235-40Q
Recall Or Safety Alert for Vitrea Enterprise Suite, VitreaAdvanced, VitreaCore (VitalConnect), and Vitrea fX, software versions prior to 6.3.3, now including 6.1.6, 6.2.3 and 6.3.0
Recall Or Safety Alert for STERRAD ® 100NX® sterilization system, reference 10104
Recall Or Safety Alert for Capture-P® Indicator RBCs, lot number 226194
Recall Or Safety Alert for Radiolucent Defibrillation Electrodes for Adults and Pediatricians Medi-Trace ™ Cadence
Recall Or Safety Alert for "ARCHITECT STAT High Sensitive troponin-I Calibrators (calibrator)", Reference 3P25-01, Lot 24057UI00 and "ARCHITECT STAT High Sensitive troponin-I Controls (controls)", Reference 3P25-01, Batches 24058UI00 and 26218UI00
Recall Or Safety Alert for Urine collection bag with belt Belly Bag® by Rusch®
Recall Or Safety Alert for Optima CT660, Brivo CT385, Discovery PET / CT 610 and Discovery PET / CT 710
Recall Or Safety Alert for Fixation ball joint for K 2.0mm Kirschner wire
Recall Or Safety Alert for KIMGUARD filters for sterilization containers, reference 68509, lot numbers MF1216 and MF1223
Recall Or Safety Alert for Variable Opening Collimator of the CyberKnife® System, serial no. C0242
Recall Or Safety Alert for Protein-specific liquid calibrator (LSP) for ADVIA ® chemistry systems 1200, 1650, 1800 and 2400
Recall Or Safety Alert for Flow Modules for the System 1 Advanced Perfusion System by Terumo®
Recall Or Safety Alert for Impactor / Extractor of the Triathlon Tibial Base Plate, ref. 6541-4-805
Recall Or Safety Alert for Braided Composite Sutures ORTHOCORD ™
Recall Or Safety Alert for GemStar infusion systems
Recall Or Safety Alert for Securmix Bolsa, Ref .: 067-400-50, lots 0812/0017, 0812/0018, and Securmix Botella, Ref .: 067-100-50, lot 0812/0019
Recall Or Safety Alert for Dilatation ™ dilatation balloon valvuloplasty catheters
Recall Or Safety Alert for Reinforced endotracheal tubes Murphy, Murphy with stylet, Magill and Magill with stylet, available in three commercial brands: Unomedical UnoFlexTM, EuromedicalTM TrachealFlexTM and PharmaPlast
Recall Or Safety Alert for Patient positioning system ExacTrac 5.x
Recall Or Safety Alert for ABX Difftrol Lot PX033, References 2062011, 2062012, 2062013, 2062203, 2062207, 2062208, 2062016, In the analyzers: ABX Pentra 120, ABX Pentra 120 Retic, ABX Pentra DF 120, ABX Pentra DX, Pentra DX Nexus and Pentra DF Nexus.
Recall Or Safety Alert for Dual Hemo Mcable
Recall Or Safety Alert for Metatarsophalangeal fusion plate 1st finger 2.4 / 2.7, AV block, medium, length 52 mm, 5 °, left
Recall Or Safety Alert for Dimension Gauge Vista Drug 4, catalog us KC460 and KC460A
Recall Or Safety Alert for "VITROS® Chemistry Products PHBR (phenobarbital) Slides", Ref .: 8221384
Recall Or Safety Alert for Plug-Oscillating Membrane used with 3100A or 3100B High Frequency Oscillating Ventilators
Recall Or Safety Alert for Thromborel S, reference and material number Siemens OUHP295 / 10446442 and OUHP495 / 10446445, in Sysmex® CS-2000i / 2100i systems, material no. Siemens 10488585
Recall Or Safety Alert for Stationary x-ray Artis digital angiography systems with VC20x software versions,
Recall Or Safety Alert for Increase CombiCup R®
Recall Or Safety Alert for Ophthalmic viscoelastic "Z Hyalin Multipack, Z Hyalin Plus Multipack and Z Hyalcoat Multipack"
Recall Or Safety Alert for Certain references and batches of the products "Bioabsorbable Anterior LCA (Anterior Cruciate Ligament) Screws", "BioZip Shoulder Anchors", and "XCEL Shoulder Anchors"
Recall Or Safety Alert for Control pumps of the AMS 800 Urinal Control System
Recall Or Safety Alert for Super Archer 0.035 inch (0.89 mm) Archer Guide, ARCSJ200W, ARCSJ260W and ARCDJ260W
Recall Or Safety Alert for Test Scrape Quadra Size 0 ", reference 01.10.10.045
Recall Or Safety Alert for item 1192177 of the product Oxoid Antimicrobial Susceptibility Testing Disc NOR10 (Norfloxacin)
Recall Or Safety Alert for item 1177571 of the product Oxoid Antimicrobial Susceptibility Testing Disc CN10 (Gentamicin)
Recall Or Safety Alert for Syngo Workflow MLR system with Radiologist Portal, software versions VB30E and VB35
Recall Or Safety Alert for Thyroid stimulating hormone (TSH) Kit, 3rd Generation, used with the Immulite® and Immulite®1000 systems
Recall Or Safety Alert for SQ / RX Impulse Generator, model 1010 and Q / TECH Programmers model 2020
Recall Or Safety Alert for Artis Zeego systems with software versions VC14J and VC21A
Recall Or Safety Alert for Family of Plum A + Infusion Pumps
Recall Or Safety Alert for Access / Access 2 Systems Immunoassay Systems, SYNCHRON LXi 725 Clinical System and UniCel DxC 600i SYNCHRON Access Clinical System
Recall Or Safety Alert for "GLU Reagent", reference 442640, all batches, used in the UniCel DxC and Synchron LX®20 analyzer systems
Recall Or Safety Alert for Pharos Vitesse Neurovascular Stent Systems
Recall Or Safety Alert for Staple release system of the MitraClip System device
Recall Or Safety Alert for Application of GenIQ Software used in Advantage Workstation or AW Server systems
Recall Or Safety Alert for Blood extraction equipment
Recall Or Safety Alert for All batches of certain references of the NEUROPATH guide catheters
Recall Or Safety Alert for "Cadisc-C Mango preparation of the terminal plate 2G" and "Cadisc-C Preparation blades of the terminal plate 2G"
Recall Or Safety Alert for Infusion systems Primary Plumset (ChemoPlum Set) Key 2, Reference nº 12196-83-24 and Clave 4, Reference nº 12194-83-24
Recall Or Safety Alert for Advanced perfusion systems 1 by Terumo®
Recall Or Safety Alert for Delta spacers Delta Revision, Delta One TT and Delta Revision TT
Recall Or Safety Alert for lot 1231742 of the product Oxoid Antimicrobial Susceptibility Testing Disc TZP36 Piperacillin \ Tazobactam
Recall Or Safety Alert for Universal charging unit Endo GIA ™ AutoSuture ™ 30 mm-2.0 mm
Recall Or Safety Alert for Conventional blood lines used with the Integra and AK machines
Recall Or Safety Alert for Conventional blood lines used with the Integra and AK machines
Recall Or Safety Alert for "Prolonsend. Extension with 3-way key "
Recall Or Safety Alert for Stationary X-ray systems of digital angiography Artis Zee / Zeego. Models: 10094135, 10094137, 10094139, 10094141, 10094142, 10094143, or 10280959, Equipped with a generator A 100 Plus model 10563420
Recall Or Safety Alert for System Advanced Perfusion System 1 of Terumo®, reference 801764
Recall Or Safety Alert for R200 C20 Icons, R200 T20 Icons, R100 Icons, MD Icons, RHD Icons, Classic RF Luminos, Fusion Luminos or Select Luminos
Recall Or Safety Alert for ISOLINE defibrillation probes models 2CR5, 2CR6 and 2CT6
Recall Or Safety Alert for Coverstainer grid for hematoxylin-eosin stain model CS100 (CS 10330)
Recall Or Safety Alert for Radiological Systems DigitalDiagnost with software version 2.1.3.
Recall Or Safety Alert for BleaseFocus anesthesia workstation, and Blease 700/900 series ventilators.
Recall Or Safety Alert for Lots 0618102 and 0619102 of the "Kit of Hemoglobia A1c", catalog number 5035C
Recall Or Safety Alert for Centricity PACS Web Diagnostic (DX) system
Recall Or Safety Alert for Discs for the analysis of antibiotic sensitivity Oxoid CPD10 (cefpodoxime)
Recall Or Safety Alert for COBAS TaqMan MTB test
Recall Or Safety Alert for Philips TAC systems "Brilliance 6", "Brilliance 10", "Brilliance 16", "Brilliance 40", "Brilliance 64", "Brilliance Big Bore" and "Brilliance iCT"
Recall Or Safety Alert for Accutrend BM-Lactate test strips, reference 03012654370
Recall Or Safety Alert for 27G disposable cannulas with 4-digit lot numbers included in the viscoelastic containers of Amvisc® and Amvisc® sodium hyaluronate
Recall Or Safety Alert for GE Centricity PACS-IW, Picture Archiving and Communication System, software versions 3.7.1 and later
Recall Or Safety Alert for ACUVUE® MOIST® 1-DAY contact lenses (etafilcon A) and ACUVUE® ADVANCE® With HYDRACLEAR (galyfilcon A)
Recall Or Safety Alert for Computed Tomography Systems SOMATOM
Recall Or Safety Alert for VIDAS D-Dimer Exclusion II, reference 30455 lot 1001399220
Recall Or Safety Alert for Peripheral drug-eluting stent Zilver PTX
Recall Or Safety Alert for Peripheral drug-eluting stent Zilver PTX
Recall Or Safety Alert for Monitor Base Unit TCM4 Series
Recall Or Safety Alert for Removal from the market of certain batches of the UniqueTemp arm and shoulder cover, due to the possibility that under certain conditions damage to the electronic system may occur.
Recall Or Safety Alert for Oxoid Antimicrobial Susceptibility Testing Discs CIP5 (Ciprofloxacin)
Recall Or Safety Alert for Leica ASP6025 tissue processor
Recall Or Safety Alert for Cartridges of the STERRAD® NX® system, REF 10133
Recall Or Safety Alert for Reagents for the ADVIA Centaur®, ADVIA Centaur® XP and ADVIA Centaur® CP systems
Recall Or Safety Alert for PopLok punch 3,5 mm -PKL-35M. Lot 256058
Recall Or Safety Alert for "Ardis Inserter" Model 3256-01, lots 52ZW, 50CL, 53BB, 55AB, 58GS, 58GT, 60JY, 62KP, 63HJ, 64EY, 68AX, 71JE and 75LE, manufactured between June 2008 and August 2011, and "Intersomatic System Ardis "
Recall Or Safety Alert for BacT / ALERT® 3D system with firmware B.40.xx
Recall Or Safety Alert for Integrated treatment console 4D (4DITC)
Recall Or Safety Alert for Clinical Chemical Analyzer AU5800
Recall Or Safety Alert for Dade® Ci-Trol® 1, Ref .: 291070, lot 528129A
Recall Or Safety Alert for Modular perfusion systems Sarns 8000, references 16405 and 16406
Recall Or Safety Alert for "Oxoid Antimicrobial Susceptibility Testing Disc": F200 (Nitrofurantoin), Reference Ct0035B, Batches 1194943 and 1198341 and F300 (Nitrofurantoin), Reference CT0036B, Batches 1191121, 1191122 and 1198342
Recall Or Safety Alert for Accent SR single-chamber pacemaker, model PM1110 and Accent DR dual-chamber pacemaker, model PM2112
Recall Or Safety Alert for External Samaritan Automatic Defibrillators (public access), PAD300 and PAD 300P Models
Recall Or Safety Alert for ELISA kit AMH Gen II, reference A79765, all batches
Recall Or Safety Alert for Alere Triage® BNP, Alere Triage® Profiler SOB ™ Panel, Alere Triage® D-dimer, Alere Triage® CardioProfiler ™ Panel, Alere Triage® Cardiac Panel, Alere Triage® TOX + MTD
Recall Or Safety Alert for Lactate membrane units (ref 942-066)
Recall Or Safety Alert for Oxoid Staphytect Plus
Recall Or Safety Alert for ExoSeal TM vascular closure device (VCD)
Recall Or Safety Alert for Infusion systems ALARIS GP
Recall Or Safety Alert for Seno Advantage workstations, versions 2.1 and 2.2, with RIS integration through the CCOW option
Recall Or Safety Alert for Urine Positive Controls CLINITEK Atlas®, Chek-Stix® Combo Pak and Chek-Stix®
Recall Or Safety Alert for Reagent Flex of TACR of Dimension
Recall Or Safety Alert for Reagent cartridges Flex® Iron (IRON), reference K3085 for the Dimension Vista® System
Recall Or Safety Alert for Dilatation catheter for ACTP EMPIRA ™ RX by Cordis
Recall Or Safety Alert for Access / Access 2 immunoassay systems, and Clinical systems SYNCHRON LXi 725 and UniCel DxC 600i SYNCHRON Access
Recall Or Safety Alert for AdVance ™ male sling system, reference 720088-02, lots between 722024001 and 790266012
Recall Or Safety Alert for MammoDiagnost DR system, reference 714040
Recall Or Safety Alert for Encore ™ 26 Advantage Kits
Recall Or Safety Alert for Brilliance Big Bore systems with TumorLOC application
Recall Or Safety Alert for Cobas b 123 FLUID PACK COOX, 200, 400 and 700
Recall Or Safety Alert for Discs for antibiotic sensitivity tests Oxoid Antimicrobial VA5 (Vancomycin)
Recall Or Safety Alert for Implantable infusion systems SynchroMed® II and SynchroMed EL
Recall Or Safety Alert for VitalTemp disposable general purpose 9 French temperature probes, models 1016 and 1016EU and VSD general anesthesia system kit, model GXXXXX64.
Recall Or Safety Alert for Extended Brilliance Workstation (EBW) Workstations with software versions 4.0.2, 4.5.2 or 4.5.3
Recall Or Safety Alert for SPRING ARM CONFIGURATIONS Visum Halogen Surgical Light, Visum LED Surgical Light and Stryker Flat Panel & Navigation Arm.
Recall Or Safety Alert for Knee and extremity systems and hip systems
Recall Or Safety Alert for Control Module IMMULITE® IGF-I, reference LGCOCM, material number Siemens 10385382, lots 0025, 025L and 0026
Recall Or Safety Alert for Essenta DR Compact
Recall Or Safety Alert for ADVIA Centaur® Calibrator C for use with the ADRIA Centaur® Ferritin assay in the ADVIA Centaur® CP System
Recall Or Safety Alert for StreamLAB® Analytical Workcell
Recall Or Safety Alert for Reagent ARCHITECT HAVAb IgG, references 6C29-20 and 6C29-25
Recall Or Safety Alert for EcoPharm Tower model MA DME 012S-80S
Recall Or Safety Alert for lot 0022 of the IMMULITE® Osteocalcin control module (LONCM)
Recall Or Safety Alert for ACUSON X150 sonographic systems, with software version 1.0, and SONOLINE G40, with software versions 1.0 and 2.0
Recall Or Safety Alert for Cobas Ampliprep (CAP) instruments, configured from source with version 3.3.5 of AMPLILINK software
Recall Or Safety Alert for HEA Beadchip Kit
Recall Or Safety Alert for MicroINR CHIPs (test strip), Ref .: CHA0025AA and CHA0025AB
Recall Or Safety Alert for IMMULITE® 2000 / IMMULITE® 2000 XPi Troponin I kit
Recall Or Safety Alert for Remel Xpect Clostridium difficile Toxin A / B, reference R24650, lot 082505 and 131988 and reference R24640, lot 141764
Recall Or Safety Alert for UniCel® DxHTM 800 Coulter cell analysis system, reference 629029 and Coulter® cellular analysis system of the Unicel® DxHTM slide stainer, reference 082775222.
Recall Or Safety Alert for STANT S31 cardiotograph with the option of monitoring maternal parameters
Recall Or Safety Alert for Protection arm against radiation Mavig Portegra 2
Recall Or Safety Alert for All the models (PAS ..., PAL ..., PVS ... and PVL ...) of the HLS Cannulas
Recall Or Safety Alert for Eclipse treatment planning system
Recall Or Safety Alert for Certain Systems TAC MX 16-Cortes
Recall Or Safety Alert for Linear Accelerators Clinac, Trilogy, Novalis Tx and Unique
Recall Or Safety Alert for Volumed® infusion pumps μVP7000 and Syramed® μSP6000
Recall Or Safety Alert for Vascular Embolectomy, Biliary and Irrigation Catheters.
Recall Or Safety Alert for Portable x-ray systems Optima XR220amx, Optima XR200amx and Brivo XR285amx, serial numbers 5555000, 5555000-2, 5555000-3, 5555000-4, 5555000-5 and 5555000-6.
Recall Or Safety Alert for Silicone oil, model RT SIL-OL 1000, Syringe 10ml, Ref .: 000000-1941-231, lot 2314
Recall Or Safety Alert for LifeCare PCA perfusion systems, reference 0F782
Recall Or Safety Alert for Fluffy screw of 6.5mm diameter, 25mm and 35mm length
Recall Or Safety Alert for Implantable Pulse Generators (GPI) EON MINI model 65-3788 and Brio model 65-6788.
Recall Or Safety Alert for Coil Flex Large Coil 4 in magnetic resonance systems MAGNETOM Skyra, Verio, Spectra and Biograph mMR.
Recall Or Safety Alert for Automatic coagulation analysis systems CS-2100i
Recall Or Safety Alert for Primary reagent cartridges ReadyPack® from the ADVIA CENTAUR BR trial for CA 15-3
Recall Or Safety Alert for "Screw Caddy" screw module, tray used to support the screws used with the anterior cervical spine plates ATLANTIS® and Premier, Ref .: 176-503, 176-504 and 1860503
Recall Or Safety Alert for ARF single-use high-power return electrode
Recall Or Safety Alert for T-piece resuscitation circuits for the Panda and Giraffe resuscitation system, manufactured between September 10, 2009 and May 10, 2012.
Recall Or Safety Alert for Eclipse ™ treatment planning system
Recall Or Safety Alert for CARESCAPE B650 monitor
Recall Or Safety Alert for Implantable Pulse Generators (GPI): "EonTM", "Eon MiniTM" and "BrioTM"
Recall Or Safety Alert for Discs of analysis of antibiotic sensitivity Oxoid FOX30 (cefoxitin)
Recall Or Safety Alert for HALOFLEX Power Generators, models 1190A-115A and 1190A-230A, all serial numbers
Recall Or Safety Alert for Single-use DUET TRS ™ Universal Straight and Articulated Loading Units
Recall Or Safety Alert for Lisubel Chek Talk TD4232 blood glucose meters
Recall Or Safety Alert for Certain references and lots of the Torque wrench: XIA3 - MANTIS REDUX - AUDIBLE SPECIALTY
Recall Or Safety Alert for Catheter for percutaneous transluminal angioplasty Armada 35 and Armada 35 LL, all lot numbers up to 783705 inclusive
Recall Or Safety Alert for ADVIA Centaur® Calibrator B for use with the ADVIA Centaur® Prolactin assay in the ADVIA Centaur® CP System
Recall Or Safety Alert for ADVIA Centaur® Calibrator B for use with the ADVIA Centaur® FSH assay in the ADVIA Centaur® or ADVIA Centaur® XP systems
Recall Or Safety Alert for PACS system (Picture Archiving and Communication System) syngo Imaging XS version VA70A
Recall Or Safety Alert for Certain batches of ADVIA Centaur® HIV 1 / O / 2 Enhanced Reagent Kits (EHIV), Ref .: 01463908
Recall Or Safety Alert for "NC Screw for NC CARES® Pillar, ZrO2 and instructions for use", Ref .: 022.2630, and "RC Screw for RC CARES® Pillar, ZrO2 and instructions for use", Ref .: 022.4630
Recall Or Safety Alert for ADVIA Centaur® BNP kit, reference numbers 02816634 and 02816138, ADVIA Centaur TSH3 Ultra kit, reference numbers 06491080 and 06491072 together with the ADVIA Centaur Multidiluent 1, reference numbers 07907174 (110313) and 07293184 (110312)
Recall Or Safety Alert for Proximate® Circular Hemorrhoidal Stapler (code PPH01) and Proximate® PPH Circular Hemorrhoidal Stapler (code PPH03).
Recall Or Safety Alert for lots 1000945440 and 1001073190 of the Product Vidas EBV VCA-EA IgG
Recall Or Safety Alert for STERRAD CycleSure 24 biological indicator, Ref. 14324 and the STERRAD kits and kits
Recall Or Safety Alert for Balloon tracheostomy tubes and Shiley ™ reusable internal cannula for measurement 8
Recall Or Safety Alert for Femur stems Profemur TL, Profemur conical, Profemur Z and Profemur Z with plasma
Recall Or Safety Alert for Infusor SV portable elastomeric infusion systems 0.5 ml / h ref. 2C1700KP, Fulfusor SV 0.5 ml / h ref. 2C4700K
Recall Or Safety Alert for Femoral Components RT-PLUS ™
Recall Or Safety Alert for Peristeen anal irrigation system
Recall Or Safety Alert for NT-proBNP Reagent Packs and Calibrators Vitros® Immunodiagnostics Products, product codes 6802157 and 6802156
Recall Or Safety Alert for RX electric operating tables, RX500, RX600 and RX700 models
Recall Or Safety Alert for Monthly maintenance kit, Ref .: CT9554 and Tubing kit for peristaltic pump, Ref .: CT4274 of the CELLTRACKS® AUTOPREP® Systems
Recall Or Safety Alert for Heat exchangers for cardioplegia PLEGIOX
Recall Or Safety Alert for Heat exchangers for cardioplegia PLEGIOX
Recall Or Safety Alert for AlligatorTM recovery devices
Recall Or Safety Alert for Ultrasound systems EPIQ 5 and EPIQ 7
Recall Or Safety Alert for Micro SSP ™ plate specifies alleles for HLA Class I DNA typing - C * 02
Recall Or Safety Alert for ACUSON X700TM ultrasound systems with software version 1.0.00, 1.0.01, 1.0.02, 1.1.00 or 1.1.02
Recall Or Safety Alert for ADVIA Centaur HIV Ag / Ac Combo (CHIV) assay, catalog number 06520528, batches finished in 038 and higher
Recall Or Safety Alert for Special Diluent from Vitros®, FS 3 Diluent Kit from Vitros®,
Recall Or Safety Alert for Ingenuity Core 128 systems with software version 3.5.5
Recall Or Safety Alert for Berichrom® Vial Protein C Activator of the Berichrom Protein C kit [OUVV175], lots 41426, 41481, 41491 and 41655
Recall Or Safety Alert for Radiation therapy treatment planning software Monaco, software version 3.10.00-3.20.00 and Focal radiation therapy treatment planning software, software version 4.64.00-4.70.00
Recall Or Safety Alert for Essenta DR Compact Systems
Recall Or Safety Alert for DigitalDiagnost systems with software version 2.0.2.
Recall Or Safety Alert for Reagent VITROS® Chemistry Products VANC and Reagent VITROS® Chemistry Products VALP
Recall Or Safety Alert for IMMULITE® / IMMULITE® 1000, IMMULITE® 2000 / IMMULITE® 2000 XPi and IMMULITE® 2500
Recall Or Safety Alert for AcrySof® CACHET® Phakic Lens (formerly called AcrySof® Phakic), models L12500, L13000, L13500 and L14000
Recall Or Safety Alert for Olimpic Cool-Cap system, serial number 1045
Recall Or Safety Alert for Biochemical products VITROS® DGXN Slides
Recall Or Safety Alert for SarnsTM High Flow Aortic Arch Cannula and SarnsTM Flexible Arterial Cannulas
Recall Or Safety Alert for Sarns Antegrade cardioplegia cannula
Recall Or Safety Alert for Carpentier-Edwards PERIMOUNT, Model 3300 and Carpentier-Edwards PERIMOUNT Magna Mitral Ease, Model 7300TFX
Recall Or Safety Alert for Legendair ™ and Supportair ™ fans
Recall Or Safety Alert for Legendair ™ and Supportair ™ fans
Recall Or Safety Alert for Workstations Extended Brilliance Workspace V4.5.2. and Systems Philips IntelliSpace Portal V4.0.1
Recall Or Safety Alert for Discs of antibiotic sensitivity analysis Oxoid ATM30 (aztreonam)
Recall Or Safety Alert for AlboGraft vascular prosthesis
Recall Or Safety Alert for CYTOSTAT tetraCHROME reagents (CD45-FITC / CD4-RD1 / CD8 ECD / CD3-PC5 and CD45-FITC / CD56-RD1 / CD19-ECD / CD3-PC5) and the tetraCXP software
Recall Or Safety Alert for ABL80 FLEX and ABL80 FLEX CO-OX analyzers
Recall Or Safety Alert for ABL80 FLEX and ABL80 FLEX CO-OX analyzers
Recall Or Safety Alert for Stationary PathFinder NXT toolholders, item numbers: 3573-1 (angled handle) and 3573-2 (straight handle)
Recall Or Safety Alert for ARCHITECT CA 19-9 XR
Recall Or Safety Alert for Echelon, OASIS, AIRIS Vento, AIRIS Vento LT, Lucent and Eterna APERTO systems, with software versions V2.1A, V2.1B, V2.2A and V3.0B
Recall Or Safety Alert for Certain references of Mass Trak immunosuppressive kits
Recall Or Safety Alert for EasyLink ™ Computing System, Version 5.0, all SP versions
Recall Or Safety Alert for Safety syringes for Monoject ™ insulin with volumes of 3 / 10mL and 1 / 2mL
Recall Or Safety Alert for Dynamis ™ and Gerialit ™ beds
Recall Or Safety Alert for surgical technique of the Modular Knee System RT-PLUS
Recall Or Safety Alert for Birdie®, Birdie® Compact and Flamingo® cranes
Recall Or Safety Alert for Lot 1174615 of the 3ml BD Preset ™ blood gas syringes, with 22Gx1 needle, Ref .: 364314
Recall Or Safety Alert for Line accelerators TrueBeam and TrueBeam STx
Recall Or Safety Alert for Reagent kits: Immulite, Immulite 1000, Immulite 2000 and Immulite 2000XPi
Recall Or Safety Alert for PRI NexGen Impactor / Proximal Femoral Puller (00-5901-026-00) and Spare Jaw (00-5901-026-40)
Recall Or Safety Alert for ABGII Modular Stems and ABGII Modular Collars, and Rejuvenate Modular Stems and Rejuvenate Modular Collars
Recall Or Safety Alert for ABGII Modular Stems and ABGII Modular Collars, and Rejuvenate Modular Stems and Rejuvenate Modular Collars
Recall Or Safety Alert for MammoDiagnost DR system
Recall Or Safety Alert for MicroScan LabPro V program 4.11 Panel Update on WalkAway systems
Recall Or Safety Alert for Infusion, FOLFusor and Intermate elastomer infusion systems
Recall Or Safety Alert for Certain batches of IMMULITE® 2000/2000 XPi Erythropoietin (L2KEPN2 / 6) and "IMMULITE® 2500 Erythropoietin (L5KEPN2)
Recall Or Safety Alert for Reactive cartridge Flex of CA19-9 (Ref. K6457), lots 11223AC, 12054BC, 12072BA and 12107AB
Recall Or Safety Alert for VITROS® 5600 Integrated Systems, software versions 1.6 and below
Recall Or Safety Alert for Titanium humeral locking screws CentroNail code 99-T744XX and 99-T786XX.
Recall Or Safety Alert for Metal-metal hip prosthesis
Recall Or Safety Alert for UniCel® DxH ™ 800 Coulter® automatic analyzer
Recall Or Safety Alert for Advantage Workstation and AW Server, with the READY View application, version 10.3.67.
Recall Or Safety Alert for Calibrator Apo A1 and B, ref. ODR3005, Lot No.: 0059C and Apo B Reagent, ref. OSR6143 and Lot No.: 9622
Recall Or Safety Alert for Injectable filler Macrolane
Recall Or Safety Alert for Biological Indicator STERRAD CycleSure 24, Ref. 14324, lot 227118
Recall Or Safety Alert for TAC equipment models "Brilliance 16" and "Brilliance 64"
Recall Or Safety Alert for BD Phoenix ™ system software
Recall Or Safety Alert for "Cordis S.MA.RT Nitinol Stent System" and "Cordis S.MA.RT CONTROL Nitinol Stent System"
Recall Or Safety Alert for Hip prosthesis RM Pressfit cup vitamys and seleXys inlay vitamys.
Recall Or Safety Alert for Linear Accelerator 4D Integrated Treatment Console (4DITC), model H51, with Eclipse 8.2 or higher versions, or a third-party system using 4DITC 8.6 or 8.8.
Recall Or Safety Alert for Cardiovascular Intervention System Philips Allura Xper FD20
Recall Or Safety Alert for Reagent Stratus CS Acute Care NT-ProBNP TestPAk, model CPBNPM,
Recall Or Safety Alert for Mobile Intensive Care Unit LS-1 with software version 1.1.6, serial numbers: 2009-0022, 2009-0023, 2009-0024 and 2009-0025
Recall Or Safety Alert for Fluid heater fastening tape enFlow IV.
Recall Or Safety Alert for Galileo Echo Blood bank analyzers, catalog number 0087000
Recall Or Safety Alert for Capsule Bravo pH and applicator system ", Ref .: FGS-0312 (5-Pak) and FGS-0313 (units), lots between 11775Q and 17101Q
Recall Or Safety Alert for Transport cases of the small and soft model, Ref .: 989803173711, of the HeartStart FR3 Automatic External Defibrillator, and distributed between May 2011 and August 2011.
Recall Or Safety Alert for All batches of Atlantis ™, Premier® and Vertex® Adjustable Bores, References, 876-460, 6860460 and 6905712
Recall Or Safety Alert for Anatomical insert of uncemented polyethylene TESS GLENOIDE
Recall Or Safety Alert for Implantable Cardiovascular Defibrillators EnTrust VR / DR / AT, models D153ATG, D153DRG, D153VRC, D154ATG, D154DRG and D154VRC
Recall Or Safety Alert for Interconnection cable for Arm C of the "Sistemas Brivo OEC 850", manufactured between August 2010 and November 2011
Recall Or Safety Alert for All versions of the TumorLOC application of the TAC Brilliance Big Bore Systems, GEMINI GXL 6, GEMINI GXL 16, GEMINI TF 16 and GEMINI TF 64
Recall Or Safety Alert for Reagent Cartridge of Magnesium K3057 Flex® Dimension Vista® Analyzer
Recall Or Safety Alert for Radiation therapy treatment planning system FastPlan Treatment Planning System
Recall Or Safety Alert for Oxoid Antimicrobial Susceptibility Testing Disc SXT25 (Sulphamethoxazole / Trimetropim)
Recall Or Safety Alert for Automatic External Defibrillator, model GE Reply
Recall Or Safety Alert for Eclipse treatment planning system, software version 7.3, 8.0, 8.1, 8.2, 8.6, 8.9 and 10.0
Recall Or Safety Alert for Philips IntelliSpace Portal system, version 4.0.0
Recall Or Safety Alert for Biomet Bone Cement V, reference 3005550011, lot 039CAJ0408
Recall Or Safety Alert for the lot 96238JN00 of the product AxSYM Free T4 Standard Calibrators and the lot 96197JN00 of the product AXSYM Free T4 Controls
Recall Or Safety Alert for "CD7 Mouse Monoclonal Antibody (clone MRQ-12)", Batches 0105-11 and 0106-05, References MAD-000913QD-8, MAD-000913QD / N, MAD-000913QD-7 and MAD-000913QD-7 / N
Recall Or Safety Alert for cyclOS Putty 1cc, 5cc and 10cc
Recall Or Safety Alert for Reagents of certain tests from different manufacturers that need to be transferred manually to the cobas c-pack MULTI cassette, to be used in the cobas c311, c501, c502, cobas Integra 400/400 plus and cobas Integra 800 systems
Recall Or Safety Alert for Endocardic stimulation probe with contractility sensor, SonRtip model PS55D
Recall Or Safety Alert for Perfusion systems
Recall Or Safety Alert for Perfusion systems
Recall Or Safety Alert for Trima Accel® CaridianBCT Disposable Line Equipment used with the Trima Accel® automatic blood collection system. All lots prior to 01UXXX manufactured before January 2012
Recall Or Safety Alert for Clinac® Linear Accelerator C Series 600C, 600CD, 6EX, DBX, 2100C, 2100CD, 2300CD, 21EX, 23EX, DMX, DHX, equipped with the software of the C series versions 2.x to 6.x
Recall Or Safety Alert for CYTO-STAT tetraCHROME reagents (CD45-FITC / CD4-RD1 / CD8-ECD / CD3-PC5 and CD45-FITC / CD56-RD1 / CD19-ECD / CD3-PC5) analyzed with the Navios flow cytometer
Recall Or Safety Alert for Oxoid Antimicrobial Susceptibility Testing Discs AMC30 Amoxycillin / Clavulanic Acid, Model CT0223B
Recall Or Safety Alert for Surgical systems da Vinci S models (IS2000) and Si (IS3000)
Recall Or Safety Alert for VITROS® Vapor Adsorption Cartridges (CAT No. 6800100)
Recall Or Safety Alert for Mechanical Stabilizers ACROBAT V, ACROBAT SUV and ACROBAT and Positioners XPose 3 and XPose 4
Recall Or Safety Alert for ABaer® hearing test with software version 5.0.17 or lower.
Recall Or Safety Alert for Certain codes and batches of the product "Codman ICP screw screw kit"
Recall Or Safety Alert for Amplification unit, models JB-116B and JB-132B, and extension unit, model MS-110B, used with the Neuro-Functional Metering System Neuromaster MEE-1000A
Recall Or Safety Alert for Reagents for immunoassay systems for the determination of CK-MB: IMMULITE® 1000 CK-MB LKMB, batches # 312, 313, IMMULITE® 1000 Turbo CK-MB LSK, IMMULITE® 2000 XPi CK-MB L2KMB, batches # 213 , 214, 215, IMMULITE 2500 CK-MB L5KCP, lots no. 136, 137
Recall Or Safety Alert for Lots 111017D and 111114C of the in vitro diagnostic reagent "Active Renin IRMA"
Recall Or Safety Alert for Adjustable radiopaque pusher CH / FR 07 / 40cm ref YN2867
Recall Or Safety Alert for Endocardic silicone cables Riata® and Riata ST ", references 1560, 1561, 1562, 1570, 1571, 1572, 1580, 1581, 1582, 1590, 1591, 1592, 7000, 7001, 7002, 7010, 7011, 7040, 7041 and 7042
Recall Or Safety Alert for Discovery NM 630 and Discovery NM / CT 670
Recall Or Safety Alert for Clinac series C or Trilogy
Recall Or Safety Alert for Nails for knee arthrodesis T2
Recall Or Safety Alert for Eclipse Treatment Planning System, software version 10 with ARIA Radiation Oncology (module RT Chart) software version 10.0.28 or 10.0.34.
Recall Or Safety Alert for Endoscopes washers Wassenburg WD440 AdaptaScope
Recall Or Safety Alert for Disposable Equipment of Red Blood Cells
Recall Or Safety Alert for Windows Server Advantage Software (AWS)
Recall Or Safety Alert for Axiom Aristos FX Plus systems
Recall Or Safety Alert for Software model 2868 for the Latitude® Zoom® model 3120 programmer and Model 6465 software for the Latitude remote monitoring system, used with implantable defibrillators from Cognis®, Teligen®, Incepta ™, Punctua ™ and Energen ™ families
Recall Or Safety Alert for Batches GA2196, GA2203, DC2221, DB2221, GA2229 and FA2237 Creatinine Flex® reagent (CREA) (DF33A) from Dimension®
Recall Or Safety Alert for DA360 knee revision systems labeled as Vanguard DA 360.
Recall Or Safety Alert for VitreaCore PET / CT function for Vitrea Enterprise Suite 1.2, Vitrea Enterprise Suite 1.3, Vitrea Enterprise Suite 6.0, Vitrea Enterprise Suite 6.1
Recall Or Safety Alert for Fluid heater enFlow IV, reference 980105VS, Model 100
Recall Or Safety Alert for Acetabular screw low profile 6.5 x 45 mm
Recall Or Safety Alert for PET / TAC Gemini TF 16 and TF 64 systems
Recall Or Safety Alert for Hemostatic guidewire with braided core for the coronary sinus SafeSheath CSG and the series of telescopic braiders SafeSheath Worley
Recall Or Safety Alert for X-ray Systems Definium 8000 and Discovery XR650 with option of Pasting (Acquisition of Full Columns and Lower Members)
Recall Or Safety Alert for Dimension Vista® systems with software version 3.4.
Recall Or Safety Alert for Dimension Vista® systems with software version 3.4.
Recall Or Safety Alert for GE OEC Flurostar 7900 system, software version 02.08.01 - 02.08.08
Recall Or Safety Alert for Senographe 2000D mammography systems
Recall Or Safety Alert for Access Ostase Calibrator, Access Ostase Quality Control and Access Ostase Reagent
Recall Or Safety Alert for Linear Accelerators Clinac, Trilogy, Trilogy Tx and Novalis Tx
Recall Or Safety Alert for Quinton BETA-CAP Adapter (8814-661001)
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1512 devices in the database
All Getinge Volista domes of Access, StandOP, Triop and Quicklock models manufactured until Decem...
Model / Serial
Aristos MX / VX AXIOM system (part number 05895003) with 3D-TOP ACSS mot. (reference 03070039)
Model / Serial
EZ1 DSP Virus Kit (48), reference 62724.
Model / Serial
Craniofacial repair implant QuickFlap Neuro
Model / Serial
Elements Shutter Unit with Buchanan heat attackers and tip for pulp heat test
Model / Serial
1507 more
3 manufacturers with a similar name
Learn more about the data
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B.Braun/Aesculap
Source
BAM
Typ Aquilion/Astion
Source
BAM
N/A
Source
FDAP
Language
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