FDADecember 22, 2022device

RipCord Syndesmosis Button, REF: STA001K

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

The hazard

Overly aggressive tension on the pull suture, while passing the medial button through a bone/soft tissue tunnel across the fibula and tibia, can exceed its strength causing it to break.

What to do

FDA enforcement status: Ongoing

Brands named

trimed

UPCs

00842188123849

Recall history

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

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