Medtronic Neuromodulation recalls

3 recent recalls on record for Medtronic Neuromodulation in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation (1)Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation (1)Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application (1)

All Medtronic Neuromodulation recalls

FDA Class II · Medical device · June 3, 2026

Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation recall — Medtronic Neuromodulation

A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

Official ID Z-2241-2026 · Official record ↗

FDA Class II · Medical device · June 3, 2026

Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation recall — Medtronic Neuromodulation

A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

Official ID Z-2240-2026 · Official record ↗

FDA Class II · Medical device · May 20, 2026

Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application recall — Medtronic Neuromodulation

Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earl…

Official ID Z-2201-2026 · Official record ↗

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.