FDASeptember 24, 2024device

Medtronic Percept RC Implantable Neurostimulators (INS), Model B35300.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

UPCs

007630008134680076300081347500763000813529

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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