Medtronic Neuromodulation recalls
All Medtronic Neuromodulation recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (16).
16 recalls published between October 23, 2024 and June 3, 2026. Most common issues: software (7).
- Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002 recall
- Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001 recall
- Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer… recall
- A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465… recall
- Restore Clinician Programmer Application (CP App)… recall
- Enhanced Verify Evaluation Handset (CFN HH90130FA) recall
- Stimulation RC Clinician Programmer Application, Model A71400… recall
- A820 myPTM Software Application associated with Medtronic SynchroMed Pump… recall
- SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps… recall
- SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps… recall
- SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps… recall
- SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps… recall
- Medtronic Recharger Kits, RS6230, RS7230, and RS5220A… recall
- Medtronic Percept RC Implantable Neurostimulators (INS), Model B35300 recall
- SynchroMed II Infusion Pump recall
- Vanta Implantable Neurostimulator (INS), Model 977006 recall