FDAJuly 8, 2025device

Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number: 92328632-09

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

The hazard

Wire break(s) have occurred in rechargeable deep brain stimulation implantable pulse generators, implanted in the submuscular pectoral location. Wire breaks prevent successful stimulation, thus requiring device removal/replacement and users may experience high monopolar impedances, undesired sensation, loss of therapy, return of symptoms and/or Bluetooth connectivity challenges.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientific neuromodulationbostonboston scientific

UPCs

0871472998504408714729985051

Recall history

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

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