Medtronic Neuromodulation Recalls

2 recalls found for Medtronic Neuromodulation. Check if any of your products are affected.

HIGHFDA DEVICE

Dec 3, 2025

Medtronic Recalls Vanta Clinician Programmer Software Over Functionality Issues

Medtronic Neuromodulation recalled 7,123 units of the Vanta Clinician Programmer Application on December 3, 2025. The software may not function as intended, potentially delaying surgical procedures. Healthcare providers and patients must stop using the software immediately.

Medtronic Neuromodulation

Complaints received

HIGHFDA DEVICE

Nov 20, 2025

Medtronic Recalls Clinician Programmer App Over High-Risk Software Issue

Medtronic Neuromodulation recalled 7,667 Clinician Programmer Applications on November 20, 2025. A software issue may prevent patients from resuming therapy, leading to a recurrence of pain symptoms. Affected models include A71100 and associated tablets.

Medtronic Neuromodulation

Software issue

Brand Statistics

Total Recalls

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