FDAApril 18, 2024device

Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG: R16 IPG KIT, REF: M365DB12160, and R32 IPG KIT, REF: M365DB12320

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

The hazard

Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may experience routine system check during IPG charging, which may cause device reset. The device reset could lead transient loss of stimulation; patients may experience undesired sensations, transient worsening of movement disorder symptoms, which may lead patient to request surgical intervention for replacement or revision.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientific neuromodulationbostonboston scientific

UPCs

87147299850448714729985051

Recall history

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

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