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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