FDAAugust 30, 2021device

OPTETRAK Comprehensive Knee System custom devices labeled as the following: a. CUSTOM OPTETRAK ANGLED PS INSERT (Product Line: 900-06-XX, 900-08-XX); b. CUSTOM OPTETRAK CC TIBIAL INSERT (Product Line: 900-23-XX, 900-30-XX); c. CUSTOM OPTETRAK CC INSERT (Product Line: 900-33-XX). NOTE: Information...

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

108858621003751088586210038210885862100399108858621004051088586210041210885862100429108858621008631088586210087010885862100887108858621008941088586210090010885862101068

Recall history

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

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