FDAFebruary 12, 2018device

Capio Standard Box 4 (Capio PC); Model #M0068312321. Intended for use in general suturing applications during open or endoscopic surgery to assist in the placement of suture material in tissues at the operative site.

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

The hazard

Potential for Capio sutures to break and /or detach.

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

UPCs

08714729257622

Recall history

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

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