FDAApril 3, 2025device

Enhanced Verify Evaluation Handset (CFN HH90130FA)

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

The hazard

Evaluation handsets may not be able to communicate with the neurostimulator due to handsets having a faster processing speed than prior handsets. An inability to connect may cause the therapy to stop being delivered and a system error will be displayed. Patient may experience return of underlying disease symptoms (e.g. overactive bladder, urinary retention, or fecal incontinence) based on their response to stimulation during the evaluation period.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

UPCs

00763000930042

Recall history

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

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