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  • Device 55
  • Manufacturer 55
  • Event 63
  • Implant 0
Name Date Date initiated Country Source
Recall Or Safety Alert for Patient monitor, Fetal monitor, B-Ultrasound Diagnosis system, Puls-Oxymeter, Electrocardiograph, Pocket Fetal Doppler, Visual Elextronic Stethoscope, Multifunctional Visual Stethoscope, Dynamic ECG-system, Digital Brain Electric Activity Mapping, Syringe pump, Infusion pump 2013-06-27 Austria BASG
Recall Or Safety Alert for Mini-Spacer with face mask 2009-03-31 Austria BASG
Recall Or Safety Alert for Skin Line Therapy 2009-04-06 Austria BASG
Recall Or Safety Alert for Hyacorp H1000 and Hyacorp HS 2013-02-13 Austria BASG
Recall Or Safety Alert for Intravascular catheter kits "ICY" for heat exchange, originally manufactured by ZOLL Medical; External cables of the JARVIK 2000 Ventricular Assist System; Separately offered screws and plates for the JARVIK 2000 Ventricular Assist system; Foam protectors added by IST CARDIOLOGY to the JARVIK 2000 Ventricular Assist System, but not provided by the manufacturer JARVIK HEART Inc.; Batteries for the operation of the JARVIK 2000 Ventricular Assist System; Endotracheal intubation tubes "ECOM", originally manufactured by CONMED Corporation; Dual lumen Bi-caval cannulae, originally manufactured by AVALON Laboratories, LLC. (AV 10013, AV 10016, AV 10019, AV 10020, AV 12100); Connectors for bi-caval cannulae with dual lumen with the marking AVALON 2013-05-28 Austria BASG
Recall Or Safety Alert for PIP, M-Implants, Rofil Implant, TiBreeze 2013-11-28 Austria BASG
Recall Or Safety Alert for Anti HIV 1.2 Cassette, HBsAg Strip/Cassette Test, HCV Strip/Cassette, HBsAb Strip/Cassette, HBcAb Strip/Cassette, PSA Strip/Cassette, Chlamydia Cassette Test 2013-11-07 Austria BASG
Recall Or Safety Alert for Cereform breast implants and sizers 2014-02-19 Austria BASG
Recall Or Safety Alert for Testicular implant REF: PR3001, PR3002, PR3003, PR3004, PR3005 and Vaginal stent REF: VS3020, VS30222, VS3024, VS3026 2015-10-15 Austria BASG
Recall Or Safety Alert for ConMed Linvatech Hall Surgical Blades 2008-03-20 Austria BASG
Recall Or Safety Alert for Breastlight 2012-09-21 Austria BASG
Recall Or Safety Alert for Plain Catgut 2008-10-17 Austria BASG
Recall Or Safety Alert for Respisense Ditto, Respisense Data 2015-07-02 Austria BASG
Recall Or Safety Alert for da Vinci Surgical Systems 2012-07-02 Austria BASG
Recall Or Safety Alert for JUVÉDERM ULTRA 4 2014-12-22 Austria BASG
Recall Or Safety Alert for Aquilon2, Aquilon, Aquilon+ and Aquilon Pro series nebulizer 2018-07-18 Austria BASG
Recall Or Safety Alert for ArgoGuide Hydrophilic Wires 2008-01-25 Austria BASG
Recall Or Safety Alert for DePuy ASR and ASR XL 2010-09-08 Austria BASG
Recall Or Safety Alert for Cristal Face 2012-01-19 Austria BASG
Recall Or Safety Alert for MITCH TRH (total hip endoprosthesis system) 2012-05-29 Austria BASG
Recall Or Safety Alert for Tibreeze 2012-02-07 Austria BASG
Recall Or Safety Alert for Samaritan PAD 500P 2015-03-11 Austria BASG
Recall Or Safety Alert for Heartware 1400, 1401XX, 1407XX, 1408 2013-06-11 Austria BASG
Recall Or Safety Alert for Sterilization envelopes, autosealable, disposable 2014-11-18 Austria BASG
Recall Or Safety Alert for GemStar™ Infusion System, Plum A+/A+ 3 Family of Infusers, LifeCare PCA™ lnfusion system , Hospira Li-ion GemStar™ Docking Station 2013-03-18 Austria BASG
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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.