FDAAugust 30, 2021device

OPTETRAK LOGIC Polyethylene Tibial Inserts, labeled as the following: a. OPTETRAK Logic PS Tibial Inserts, Product Line 02-012-35-XXXX; b. OPTETRAK Logic PSC Tibial Inserts, Product Line 02-012-44-XXXX; c. OPTETRAK Logic CR Tibial Inserts, Product Line 02-012-47-XXXX; d. OPTETRAK Logic CR Slope +...

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

020123500091088586200164102012350011108858620016580201235001310885862001665020123500151088586200167202012351009108858620016890201235101110885862001696

Recall history

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

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OPTETRAK LOGIC Polyethylene Tibial Inserts, labeled as the following: a. OPTETRAK Logic PS Tibial Inserts, Product Line 02-012-35-XXXX; b. OPTETRAK Logic PSC Tibial Inserts, Product Line 02-012-44-XXXX; c. OPTETRAK Logic CR Tibial Inserts, Product Line 02-012-47-XXXX; d. OPTETRAK Logic CR Slope +... — Recall Details · AllClear