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Medtronic Neuromodulation recalls - full list & free alerts

5 official U.S. recalls involving Medtronic Neuromodulation in the last 12 months, most recently on 2026-06-03.

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Full list (5)

Medtronic Neuromodulation: Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor
Medical DevicesFDA (device) · 2026-06-03 · Class II
Medtronic Neuromodulation: Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor
Medical DevicesFDA (device) · 2026-06-03 · Class II
Medtronic Neuromodulation: Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900
Medical DevicesFDA (device) · 2026-05-20 · Class II
Medtronic Neuromodulation: A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and oper
Medical DevicesFDA (device) · 2026-01-21 · Class II
Medtronic Neuromodulation: Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET
Medical DevicesFDA (device) · 2025-12-31 · Class II