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  • Device 27
  • Manufacturer 92
  • Event 253
  • Implant 4
Name Date Date initiated Country Source
Recall of Device Recall ESSENTIO MRI EL DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall PROPONENT SR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall PROPONENT DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall PROPONENT EL DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall PROPONENT VDD SL Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall PROPONENT MRI Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall Ellipse 2016-03-31 United States USFDA
Recall of Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller 2017-03-30 United States USFDA
Recall of Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller 2017-03-30 United States USFDA
Recall of Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller 2017-03-30 United States USFDA
Recall of Device Recall ACCOLADE SR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ACCOLADE DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ACCOLADE EL DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ACCOLADE MRI SR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ACCOLADE MRI DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ALTRUA 2 EL DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall VISIONIST CRTP Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall VISIONIST X4 CRTP Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ESSENTIO SR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ESSENTIO DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ESSENTIO MRI SR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ESSENTIO MRI DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ESSENTIO EL DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall AngioSeal 2006-06-07 United States USFDA
Field Safety Notices about Ellipse DR, VR 2014-08-19 Serbia ALIMSA
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About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

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.