Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Restore Clinician Programmer Application Software Recalled by Medtronic Neuromodulation Due to The original version of the A71100 Restore Clinician...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Neuromodulation directly.
Affected Products
Restore Clinician Programmer Application Software, model number A71100, used with the Restore Neurostimulators.
Quantity: 2,408 devices
Why Was This Recalled?
The original version of the A71100 Restore Clinician Programmer Application has been identified to have a compatibility issue with some legacy clinician programmer software resulting in the programmer having an inability to establish communication with the implanted neurostimulators.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Neuromodulation
Medtronic Neuromodulation has 95 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report