FDAAugust 30, 2021device

OPTETRAK Comprehensive Knee System, labeled as the following: a. OPTETRAK All-polyethylene CR Tibial Components, with Product Line Numbers: 200-11-XX, 200-12-XX, 200-13-XX, 200-14-XX, 200-15-XX, 200-16-XX; b. OPTETRAK All-polyethylene PS Tibial Components, with Product Line Numbers: 204-11-XX, 20...

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

108858620399341088586203996510885862039972108858620399891088586203999610885862040008108858620400151088586204003910885862040046108858620400531088586204007710885862040084

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, labeled as the following: a. OPTETRAK All-polyethylene CR Tibial Components, with Product Line Numbers: 200-11-XX, 200-12-XX, 200-13-XX, 200-14-XX, 200-15-XX, 200-16-XX; b. OPTETRAK All-polyethylene PS Tibial Components, with Product Line Numbers: 204-11-XX, 20... — Recall Details · AllClear