FDANovember 24, 2017device

U2 Total Knee System Tibial Insert, Posterior Stabilized, #3, 11mm Thick Catalogue number 2303-3032 The U2 Total Knee system is indicated in knee arthroplasty for reduction or relief of pain and/or improved knee function in skeletally mature patients with severe knee pain and disability due to rh...

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

The hazard

UOC received a customer compliant report from our distributor on October 31, 2017 which stated that contents of the package do not match the product labeling.

What to do

FDA enforcement status: Terminated

Brands named

united orthopedicunited

Recall history

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

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