How do I know if my Medtronic Neuromodulation product is part of a recall?

Compare the lot code, UPC, model number or dates on your product with the official recall notice linked on this page. Our lot/UPC checker searches the official text but is not a guarantee.

What should I do if my Medtronic Neuromodulation product is recalled?

Follow the instructions in the official notice from the agency (FDA, USDA FSIS, CPSC or NHTSA), such as stopping use, returning or discarding the product, or contacting the company.

Is Medtronic Neuromodulation recalled? 5 official recalls

Official U.S. agency records list 5 recalls involving Medtronic Neuromodulation in the last 12 months, most recently on 2026-06-03. Check each official notice for the exact products, lot codes and dates affected.

Check a lot code, UPC or model number

This is not a guarantee; check the official notice.

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

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Is Medtronic Neuromodulation recalled?

Recalls (5)