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List view Cards view
  • Device 27
  • Manufacturer 92
  • Event 253
  • Implant 4
Name Date Date initiated Country Source
Recall of St Jude Medical Ellipse VR CD1377-36C Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2277-36 Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1377-36QC Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2377-36QC Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2377-36 Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1277-36 Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1377-36 Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2377-36Q Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1277-36Q Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse VR CD1377-36Q Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2277-36Q Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Ellipse DR CD2377-36C Implantable Defibrillator 2014-08-19 New Zealand NZMMDSA
Recall of St Jude Medical Merlin @ Home 2014-12-24 New Zealand NZMMDSA
Recall of VALITUDE X4 CRT-P U128 2017-12-15 New Zealand NZMMDSA
Recall of PROPONENT MRI SR Pacemaker L210 2017-12-15 New Zealand NZMMDSA
Recall of VISIONIST CRT-P U225 2017-12-15 New Zealand NZMMDSA
Recall of ACCOLADE MRI SR Pacemaker L310 2017-12-15 New Zealand NZMMDSA
Recall of Device Recall ACCOLADE MRI EL DR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall Merlinhome RF Remote Monitoring Transmitter, Model EX1150, with software versions 6.1M or 7.0 2014-12-18 United States USFDA
Recall of Device Recall TactiSys Quartz Pack, PN004 400 2014-11-25 United States USFDA
Recall of Device Recall Optisure HV lead 2015-11-03 United States USFDA
Recall of Device Recall VALITUDE CRTP Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall VALITUDE X4 CRTP Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ALTRUA 2 SR Pacemaker 2017-12-07 United States USFDA
Recall of Device Recall ALTRUA 2 DR Pacemaker 2017-12-07 United States USFDA
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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.