Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Percept BrainSense Implantable Neurostimulator (INS) Recalled by Medtronic Neuromodulation Due to The Implantable Neurostimulator (INS) cannot communicate with the...
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
Percept BrainSense Implantable Neurostimulator (INS), Model B35200
Quantity: 14164 units
Why Was This Recalled?
The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system.
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