Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic Percept RC Implantable Neurostimulators (INS) Recalled by Medtronic Neuromodulation Due to A limited number of Percept RC Implantable Neurostimulators...
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
Medtronic Percept RC Implantable Neurostimulators (INS), Model B35300.
Quantity: 39 units
Why Was This Recalled?
A limited number of Percept RC Implantable Neurostimulators (INS), Model B35300 will not be able to communicate with the A610 DBS Clinician Programmer Application upon use and an "Invalid Device" message will appear.
Where Was This Sold?
International distribution to the countries of Germany, UK, and Israel.
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