FDAMay 14, 2018device

Foundation Modular Femoral Stem, Part Number, 220-10-110. Knee prosthesis component. The Foundation Revision Knee is a total knee system indicated as knee joint replacement for patients suffering from pain and dysfunction.

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

The hazard

After receipt of a product complaint for the labeling, it was determined that this device does not have FDA clearance.

What to do

FDA enforcement status: Terminated

Brands named

encore medical lpencoreencore medical

Recall history

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

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