Medtronic Neuromodulation

Medtronic Neuromodulation: 4 recalls listed since January 2026 across FDA.

By year

Wrong lead or percutaneous extension selected.

Moderate riskFDAOct 22, 2026Device defect

The Medtronic Pocket Adaptor Kits are labeled with incorrect Use-By-Dates.

Moderate riskFDAMay 28, 2026Labeling error

The software may display infusion steps out of order, causing the schedule not to be delivered at the intended time.

Moderate riskFDAMay 14, 2026Software defect

The A71200 Vanta Clinician Programmer Application may not function as intended, potentially causing a prolonged or postponed surgical procedure.

Moderate riskFDAJan 9, 2026Device defect