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FDAApril 18, 2019device

Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420322 Phase 3 Femoral Drill Guide Medium

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

The hazard

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

Recall history

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

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