FDANovember 8, 2021device

Boston Scientific ROTAPRO, Rotational Atherectomy System Console, Model numbers H74939309010 (US) and H74939309030 (EU).

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

The hazard

Manufacturing instructions did not include the directions to not retest the pneumatic kit component of the ROTAPRO console upon failure, an internal nonconformity.

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

UPCs

0871472997507608714729975151

Recall history

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

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Boston Scientific ROTAPRO, Rotational Atherectomy System Console, Model numbers H74939309010 (US) and H74939309030 (EU). — Recall Details · AllClear