Medtronic Neuromodulation: 54 recalls on record

Recalls filed with 1 agency: FDA (54).

First recall on record: December 19, 2012. Most recent: June 3, 2026.

Risk classification: Class I: 14 · Class II: 39 · Class III: 1

Most recent recalls

DateAgencyProduct
May 27, 2015FDAMedtronic DBS Extension Kit for Deep Brain Stimulation, Models 37085 and 37086. SterileZ-1617-2015
March 4, 2015FDAThe Medtronic, Quadripolar ITREL 3 IPG, Model 7425, is a multiprogrammable device designe…Z-1147-2015
August 27, 2014FDAMedtronic, Activa PC, Model 37601, Method of Sterilization: Ethylene Oxide, Single Use On…Z-2259-2014
August 20, 2014FDAMedtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Cath…Z-2172-2014
August 6, 2014FDAMedtronic Nexdrive Micropositioning Drive. Models Ml-1000 and Ml-2000. For use in co…Z-2118-2014
June 11, 2014FDAMedtronic Model 8780 Ascenda Intrathecal Catheter. The implantable Medtronic Model 878…Z-1723-2014
May 14, 2014FDAMedtronic SynchroMed¿ II Implantable Drug Infusion Pump, Model 8637-20, 8637-40. The i…Z-1570-2014
May 14, 2014FDARefill Kit 8551/856X (includes Models 8561, 8562 and 8564) for use with Medtronic Implant…Z-1568-2014
May 7, 2014FDAMedtronic Activa RC (37612), Activa PC (37601), Activa SC (37602), Activa SC (37603), Ac…Z-1525-2014
May 7, 2014FDAMedtronic, External neurostimulator, ENS (37021) & ENS (37022). Including the external …Z-1526-2014
May 7, 2014FDAMedtronic neurostimulators. Restore (37711), RestoreADVANCED (37713), RestoreADVANCED Sur…Z-1524-2014
November 20, 2013FDAMedtronic RestoreUltra, model 37712, and RestoreSensor, model 37714, Multi-program Rechar…Z-0278-2014
November 20, 2013FDAMedtronic Activa PC, model 37601, and Activa RC, model 37612, Activa SC, models 37602 and…Z-0279-2014
November 6, 2013FDAMedtronic Activa PC, model 37601, and Activa RC, model 37612, Multi-program Rechargeable …Z-0125-2014
November 6, 2013FDAMedtronic RestoreUltra, model 37712, and RestoreSensor, model 37714, Multi-program Rechar…Z-0124-2014
July 3, 2013FDAMedtronic Intrathecal Catheter, model 8731SC. Contents: 38.1-cm spinal segment with len…Z-1576-2013
July 3, 2013FDAMedtronic SynchroMed II, Model 8637, (The SynchroMed II Pump is supplied in 20 ml or 40 m…Z-1570-2013
July 3, 2013FDAMedtronic INDURA 1P Intrathecal Catheter, model 8709SC. Contents: 81.4-cm catheter with…Z-1575-2013
July 3, 2013FDAMedtronic SynchroMed EL Programmable pumps, Models 8626, 8626L, 8627, 8627L, (The Synchro…Z-1580-2013
July 3, 2013FDAMedtronic Sutureless Pump Connector Revision Kit, model 8578. Contents: catheter interf…Z-1573-2013
July 3, 2013FDAMedtronic SynchroMed II, Model 8637, (The SynchroMed II Pump is supplied in 20 ml or 40 m…Z-1579-2013
July 3, 2013FDAMedtronic Intrathecal Catheter Pump Segment Revision Kit, model 8596SC. Contents: 60-cm…Z-1574-2013
July 3, 2013FDAMedtronic SynchroMed EL Programmable pumps, Models 8626, 8626L, 8627, 8627L, (The Synchro…Z-1571-2013
May 8, 2013FDAMedtronic DBS Therapy for Dystonia Kit, models 3317, 3319, 3337 and 3339. Sterile and N…Z-1191-2013
May 8, 2013FDAMedtronic DBS Lead Kit for Deep Brain Stimulation, models 3387, 3387S, 3389, 3389S, 3391,…Z-1190-2013

Questions about this company

How many recalls does Medtronic Neuromodulation have?
Recalert has 54 U.S. recalls on record for Medtronic Neuromodulation, published between December 19, 2012 and June 3, 2026.
Which agencies have handled Medtronic Neuromodulation recalls?
Medtronic Neuromodulation appears as the recalling firm in recalls from: FDA (54).

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