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Manufacturers
Device Technologies Australia Pty Ltd
Manufacturer Parent Company (2017)
Device Technologies Australia Pty. Ltd.
Source
DHTGA
91 Events
Recall of Nutriline and Nutriline Twinflo Peripherally inserted central catheters (PICC)NUTRILINE W STYLET AND MICROFLASH
Recall of Symmetry Surgical/Olsen – Single Use Electrocautery Forceps/Pencils/Cords
Recall of da Vinci Xi EndoWrist Stapler Release Kit (SRK)
Recall of Premicath Neonatal PICC with Stylet Premicath with Stylet
Recall of NON REBREATHE MASK
Recall of da Vinci X Patient Side Cart Arm Controller Joint Circuit Boards
Recall of CareFusion Vyntus Body with Option Diffusion
Recall of da Vinci Xi Surgical System P6b Software
Recall of SynCardia Freedom Driver System (a component of the SynCardia temporary Total Artificial Heart System)
Recall of V-PRO 60 Low Temperature Sterilisation System with VAPROX HC Sterilant Distributed between 31 July 2014 and 17 August 2017
Recall of Ceiling Unit CU5001/3 and CU 3-21/23
Recall of Lentis Foldable Intraocular Lenses (IOL)
Recall of Vygon Umbilical Catheters
Recall of Corpuls3 CO2 Disposable Naso-oral Adaptor Capone
Recall of Laser photocoagulator Easyret software version 1.03
Recall of Corpuls3 defibrillator/monitoring unit – Printer Paper
Recall of SwiveLock SP Suture Anchor
Recall of da Vinci Xi EndoWrist Stapler Release Kit (SRK)
Recall of Left Double Lumen Endobronchial Tube with Parker Flex-Tip
Recall of Roth Net Standard Polyp Retriever U-711151
Recall of Intuitive Surgical Endoscope Instrument Control System - da Vinci Xi Surgical System with P5 software
Recall of Arthrex ITD Articulating Arm 300 + 350MM
Recall of da Vinci Xi EndoWrist Stapler 45 Instrument
Recall of da Vinci Xi EndoWrist Stapler
Recall of V-PRO 1, V-PRO 1 Plus, V-PRO maX Low Temperature Sterilisation Systems Manufactured between 2 January 2014 and 2 May 2016
Recall of da Vinci Xi 5mm-8mm Universal Cannula Seal and da Vinci Xi 12mm & Stapler Universal Cannula SealUniversal Seals, 5mm-8mm
Recall of da Vinci Si and Xi Surgical System - Touchpad Compact Flashcardsda Vinci Si/Xi SSC Touchpad
Recall of STERIS Quick Connects (used with the Steris System 1 Express and System 1 Plus sterilisers)
Recall of Horizon Medical Imaging (HMI) product versions 4.6.1 up to and including 11.9 and McKesson Radiology (MR) 12.0 and 12.1.1(Radiology Picture archiving and communication system)
Recall of Steris Amsco Warming Cabinet; War Cab Pre Glass Dual 24" 230V mobile; War Cab PTD Glass SGL 18” 230V
Recall of PS900 Power Module supplied with 12 Lead ECG Interp. 210mm Basic Monitors
Recall of da Vinci Xi instrument & accessoriesAffected instruments:0 deg, 8mm Endoscope, IS4000
Recall of Arcadophta SARL– Arcotane 5ml
Recall of Various surgical instruments actuated by the da Vinci Si Single Site Grip Release mechanism
Recall of Arceole C3F8 and SF6
Recall of Vygon SA – Y connector code 884.08(tubing connector)
Recall of Da Vinci Xi Surgical System - Breakage of input disks of Endowrist instruments Reprocessing Instruction: 551708-01
Recall of TOPCON – 3D Optical Coherence Tomography 3D OCT-1 MAESTRO machines
Recall of CareFusion - AVEA Ventilator
Recall of Corpatch Easy Paediatric (defibrillator electrodes)
Recall of Talon Grasping Device(Used for retrieval of foreign bodies, tissue specimens, stones or calculi in endoscopic procedures of the gastrointestinal tract)
Recall of Microtek Medical System Drapes used with da Vinci, da Vinci Si, da Vinci Si/S Systems
Recall of STERIS Caviwave Pro Ultrasonic Cleaning System (used to wash instruments and accessories prior to final disinfection and sterilisation)
Recall of Intuitive Surgical Inc. da Vinci Xi Surgical System Patient Cart Arms
Recall of da Vinci Si EndoWrist One Vessel Sealer and da Vinci Xi EndoWrist Vessel Sealer da Vinci Si EndoWrist One Vessel Sealer
Recall of Bead Block (Embolic Bead)
Recall of Intuitive Harmonic ACE Instruments (used with the da Vinci Standard, S, and Si Surgical Systems)
Recall of 5mm and 8mm Harmonic ACE Instruments IFU (for use with 5mm Harmonic ACE instruments (PNs 400274 and 400275) 8mm Harmonic ACE instruments (PNs 420274 and 420275) and Harmonic ACE Curved Shears Disposable Insert (PN 400272) used with the da Vinci Standard, S, and Si Surgical Systems.
Recall of LENTIS HydroSmart Foldable Intraocular Lenses in Glass Vials IOL
Recall of da Vinci Standard Surgical System, da Vinci S Surgical System, da Vinci Si Surgical System, da Vinci Si-e Surgical System including all instruments and accessories used with the da Vinci surgical systems
Recall of STERIS 5085 and 5085SRT Surgical Table
Recall of Endo Wrist One Vessel Sealer (INS-410322) for the da Vinci Si (IS3000) Surgical System(Single use active endotherapy device used in endoscopic procedures for cutting and or coagulating tissue)
Recall of Defibrillator/pacer SLIM corpuls3
Recall of Horizon Cardiology Hemo – versions 13.0 and 13.1 (cardiology/cath lab information management system)
Recall of Intuitive Surgical Battery Box of the da Vinci STM and da Vinci SiTM Surgical Systems
Recall of STERIS 4085, 4085 SS and 4085 Feather Weight Leg Section (FLWS) Surgical tables
Recall of Specular Microscope SP-1P (non-invasive photographic microscope)
Recall of Large Clip Applier for use with the da Vinci STM and da Vinci SiTM
Recall of Slide-in Plug Adaptor for Charger used with Haag Streit UK Perkins MkIII Tonometer Tonometer
Recall of Horizon Cardiology Hemo1 – versions 12.2 HF4 and earlier(used for acquiring, displaying and reviewing haemodynamic parameters (vital signs) in cardiac catheterisation laboratories)
Recall of HOYA Corporation (PENTAX Medical) – Gas/Water Feeding Valve
Recall of Horizon Medical Imaging Products Versions 4.6.1 up to and including 11.9 and McKesson Radiology 12.0 (Radiology picture archiving and communication system)
Recall of Horizon Medical Imaging products versions 4.5 up to and including 11.9 and McKesson Radiology 12.0 (Radiology picture archiving and communication system)
Recall of Intuitive Surgical Inc. – 5mm Curved Cannula for Single-Site Instruments for da Vinci Surgical Systems
Recall of Head Positioning Devices
Recall of Cup Removal Instruments (Reusable surgical instrument used to remove an acetabular cup with minimal loss of bone)
Recall of Horizon Medical Imaging (HMI) products software versions 4.5 to and including 11.9 (Radiology picture archiving and communication system)
Recall of Large and Mega Needle Driver Endowrist Instruments for da Vinci Surgical Systems
Recall of Patient Side Manipulators - da Vinci S, Si, Si-e Surgical System (robotic surgical unit)Manufactured from October 2012 to April 2013
Recall of IS3000 HD Lamp Modules with metal finish (endoscopic illumination system used with the da Vinci Si Vision Cart System which is a robotic surgical system)
Recall of da Vinci S Surgical System, IS2000; da Vinci Si Surgical System IS3000
Recall of Vygon Nutrisafe Syringe Feeding Pumps
Recall of Reliance Endoscope Processing System (EPS) used with FUJINON G5 and G8 Type Flexible GI Endoscopes
Recall of Single-Site Bipolar Maryland and Single-Site Curved Needle Driver (Reusable endotherapy device with an endoscope)
Recall of Vygon Purple Nutrisafe Feeding Tube 10 FR
Recall of Gas/Water Feeding Valve – PTX-OF-B194 (Used with PENTAX GI Video Endoscopes - 90i/90K series and i10/K10 series )
Recall of Endowrist Instruments and Accessories for the da Vinci Surgical Systems (Used in endoscopic procedures)
Recall of Intuitive Surgical 5mm Cannula and 5mm Flared Cannula (Reusable endotherapy cannula)
Recall of 5L and 10L Prolystica Ultra Concentrate Alkaline Detergent
Recall of 8 mm Fenestrated Bipolar Forceps used with da Vinci Standard System (IS1200)
Recall of Intuitive Surgical EndoWrist Instrument Hot Shears Monopolar Curved Scissors
Recall of STF Load Check Indicators (ultrasonic bath efficacy indicator)
Recall of Sterile Adapter for use with the da Vinci S, da Vinci Si, da Vinci Si-e (robotic surgical system)
Recall of IPAD Defib Pad, CU-CUA0512F (used with I-PAD NF 1200 Defibrillator)
Recall of Corpuls Defibrillator (Automated defibrillator).
Recall of Steris Reliance 130L Cart Washer (decontamination washer utensil)
Recall of Haag-Streit International -Tonometer Measuring Prisms (an ophthalmic device used to measure eye ocular pressure/tension).
Recall of Bolton Surgical - Sims Speculum D/E Insulated Large 33 x 38 mm 18.5cm
Recall of Arthrex and Andreas Hettich Rotofix 32A Centrifuge, An in vitro diagnostic medical device (IVD)
Recall of Intuitive Surgical Version 12 Tip Cover for 8mm Monopolar Curved Scissors (endotherapy scissors)
Recall of Pentax PTX-EG-387UTK Ultrasound Video Gastroscope (flexible gastroduodenoscope)
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91 devices in the database
Nutriline and Nutriline Twinflo Peripherally inserted central catheters (PICC)NUTRILINE W STYLET ...
Model / Serial
Nutriline and Nutriline Twinflo Peripherally inserted central catheters (PICC)NUTRILINE W STYLET AND MICROFLASH Product Code: VY-1252.030 NUTRILINE TWINFLO WITH STYLET Product Code: VY-1252.230 ARTG Number: 141227(Device Technologies Australia Pty Ltd - Catheter, intravascular, general-purpose)
Symmetry Surgical/Olsen – Single Use Electrocautery Forceps/Pencils/Cords
Model / Serial
Symmetry Surgical/Olsen – Single Use Electrocautery Forceps/Pencils/Cords ARTG Numbers: 214571, 214834, 214569
da Vinci Xi EndoWrist Stapler Release Kit (SRK)
Model / Serial
da Vinci Xi EndoWrist Stapler Release Kit (SRK)Product Name: IS4000 EndoWrist Stapler 45 – Stapler Release KitObsolete Product Code: INS-381215New Product Code: INS-381215-03Part Number: 381215-02ARTG Number: 228401(Device Technologies Australia - Wrench, surgical)
Premicath Neonatal PICC with Stylet Premicath with Stylet
Model / Serial
Premicath Neonatal PICC with Stylet Premicath with Stylet Product Code: VY-1261.153 Premicath 1FR 20cm Split NeedleProduct Code: Vy-1261.203 Premicath with Stylette Product Code: VY-1261.205 Premicath W Pink Hub Secure Device Product Code: VY-1261.207 Premicath 1FR 28g 30cm w/stylet Product Code: VY-1261.306 ARTG Number: 141227(Device Technologies Australia Pty Ltd - Catheter, intravascular, general-purpose)
NON REBREATHE MASK
Model / Serial
NON REBREATHE MASKProduct Code: WL-PB23401-1VBatch Numbers: 1703020228 and 1703020368ARTG Number: 133120 (Device Technologies Australia - Mask, non-rebreathing, air/oxygen)
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Device Technologies Australia Pty Ltd
Manufacturer Parent Company (2017)
Device Technologies Australia Pty. Ltd.
Source
RLMPH
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