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  • Device 178
  • Manufacturer 0
  • Event 162
  • Implant 50
Name Date Date initiated Country Source
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 SynchroMed II Implantable Infusion Pump 2013-06-03 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump 2008-08-25 United States USFDA
Recall of Device Recall SynchroMed EL Implantable Infusion Pump 2013-06-03 United States USFDA
Recall of 8709SC: Indura 1P 2008-04-14 United States USFDA
Recall of Device Recall Medtronic SynchroMed II 2011-07-05 United States USFDA
Recall of Device Recall SynchroMed II implantable infusion pump 2012-11-09 United States USFDA
Recall of Device Recall SynchroMed II Implantable Drug Infusion Pump 2014-02-26 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Infusion Pump 2008-08-25 United States USFDA
Recall of Device Recall SynchroMed II Implantable Infusion Pump 2013-06-03 United States USFDA
Recall of 8731SC: Intrathecal Catheter 2008-04-14 United States USFDA
Recall of Device Recall SynchroMed II implantable drug infusion pump 2017-02-09 United States USFDA
Recall of 8596SC: Intrathecal Catheter Pump Segment Revision Kit 2008-04-14 United States USFDA
Recall of Device Recall Synchromed II 2004-05-11 United States USFDA
Recall of Medtronic SynchroMed II Implantable Infusion Pumps 2015-04-10 United States USFDA
Recall of Device Recall 8870 Software Application Card Version AAA 02 2004-08-24 United States USFDA
Recall of Medtronic Implantable Programmable Infusion Pumps 2014-04-04 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL 2006-06-06 United States USFDA
Recall of Device Recall SynchroMed II Implantable Infusion Pump 2013-06-03 United States USFDA
Recall of Device Recall SynchroMed EL implantable infusion pump 2012-11-09 United States USFDA
Recall of Device Recall Ascenda Intrathecal Catheter 2014-07-11 United States USFDA
Recall of 8578: Suturless Pump Connector Revision Kit 2008-04-14 United States USFDA
Recall of Device Recall Medtronic, Model 8870, Application Software Card 2012-03-12 United States USFDA
Recall of Device Recall Medtronic SynchroMed EL Programmable Pump 2008-08-25 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.