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  • Device 178
  • Manufacturer 0
  • Event 162
  • Implant 50
Name Date Date initiated Country Source
Recall of Device Recall Synchromed II 2004-05-11 United States USFDA
Recall of Device Recall 8870 Software Application Card Version AAA 02 2004-08-24 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL 2006-06-06 United States USFDA
Recall of 8731SC: Intrathecal Catheter 2008-04-14 United States USFDA
Recall of 8709SC: Indura 1P 2008-04-14 United States USFDA
Recall of 8596SC: Intrathecal Catheter Pump Segment Revision Kit 2008-04-14 United States USFDA
Recall of 8578: Suturless Pump Connector Revision Kit 2008-04-14 United States USFDA
Recall of SYNCHROMED II - PROGRAMMABLE PUMP 2008-06-18 Canada HC
Recall of Device Recall Medtronic SynchroMed II Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall Medtronic SynchroMed II Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Infusion Pump 2008-08-25 United States USFDA
Recall of Device Recall N'Vision software Application Card 2009-03-23 United States USFDA
Recall of Device Recall SYNCHROMED II PROGRAMMABLE DRUG INFUSION SYSTEM 2009-07-01 United States USFDA
Recall of Device Recall Medtronic Sutureless Pump Connector Revision Kit 2009-08-27 United States USFDA
Recall of Device Recall Medtronic Intrathecal Catheter Pump Segment Revision Kit 2009-08-27 United States USFDA
Recall of Device Recall Medtronic Intrathecal Catheter 2009-08-27 United States USFDA
Recall of Device Recall Medtronic Indura 1P Intrathecal Catheter 2009-08-27 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL implantable drug pump 2011-01-14 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.

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