Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept Recalled by Medtronic Neuromodulation Due to A software anomaly in the A620 Patient Programmer...
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 PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep brain stimulation therapy. It is indicated for DBS treatment for Parkinson s disease, essential tremor, dystonia, obsessive-compulsive disorder, and epilepsy.
Quantity: 12 devices
Why Was This Recalled?
A software anomaly in the A620 Patient Programmer application was identified that results in failure to connect with the Percept PC device.
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