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Zimmer Biomet, Inc. recalls Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420322 Phase 3 Femoral Drill Gu
Recalled June 12, 2019 · FDA recall Z-1737-2019 · Zimmer Biomet
Hazard
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion. · FDA Class II
Units
10 units
Sold at
CA, IN, LA, NM, NY, TX, WI Foreign: CANADA, AUSTRALIA, JAPAN, NETHERLANDS
Description
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
Product
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420322 Phase 3 Femoral Drill Guide Medium
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →