FDAJuly 11, 2013device

AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10 mm x 24 mm). For orthopedic use in ligament reconstruction.

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

The hazard

Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.

What to do

FDA enforcement status: Terminated

Brands named

cayenne medicalcayenne

Recall history

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

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