FDAAugust 30, 2021device

ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX, 256-13-XX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

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

The hazard

Inserts were packaged in vacuum bags that lacked an additional oxygen barrier layer.

What to do

FDA enforcement status: Ongoing

Brands named

exactech

UPCs

10885862066633

Recall history

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

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ARTHROFOCUS Polyethylene Tibial Inserts (Product Line: 256-12-XX, 256-13-XX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022. — Recall Details · AllClear