FDAFebruary 12, 2018device

PFR Kit- Pinnacle, Posterior; Model #M0068317100. Indicated for tissue reinforcement in women with pelvic organ prolapse.

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

08714729784449

Recall history

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

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PFR Kit- Pinnacle, Posterior; Model #M0068317100. Indicated for tissue reinforcement in women with pelvic organ prolapse. — Recall Details · AllClear