FDAApril 18, 2024device

OPTETRAK, Advanced Patella, 3 Peg Implant, Item Numbers: a) 200-07-26, 26MM; b) 200-07-29, 29MM; c) 200-07-32, 32MM; d) 200-07-35, 35MM; e) 200-07-38, 38MM

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

The hazard

Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.

What to do

FDA enforcement status: Ongoing

Brands named

exactech

UPCs

1088586231426010885862314277108858623142841088586231429110885862314307

Recall history

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

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