FDAAugust 30, 2021device

OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial Components (Product Line: 02-012-38-XXXX). 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

020123810091088586200235802012381011108858620023650201238101310885862002372020123810151088586200238902012381509108858621787940201238151110885862178800

Recall history

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

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OPTETRAK Comprehensive Knee System including OPTETRAK Logic RBK PS Tibial Components (Product Line: 02-012-38-XXXX). NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022. — Recall Details · AllClear