FDAAugust 28, 2025device

Extractor Pro RX Retrieval Balloon Catheter; UPN (REF): (1) M00547030 (9-12mm Below), (2) M00547000 (9-12mm Above);

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

The hazard

The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

0871472979028008714729790266

Recall history

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

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