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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
Related Medical Device Recalls
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Z-1738-2019 - Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420323 Phase 3 Femoral Drill Guide Large 2 06/06/2019 FEI # 1000220733
Zimmer Biomet, Inc.
Z-1740-2019 - Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421060 Phase 3 Femoral Drill Guide Extra Small 2 06/06/2019 FEI # 1000220733
Zimmer Biomet, Inc.
Z-1741-2019 - Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421930 System Domed Lateral Femoral Drill Guide Small 2 06/06/2019 FEI # 1000220733
Zimmer Biomet, Inc.
Z-1736-2019 - Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420321 Phase 3 Femoral Drill Guide Small 2 06/06/2019 FEI # 1000220733
Zimmer Biomet, Inc.
Z-1737-2019 - Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420322 Phase 3 Femoral Drill Guide Medium 2 06/06/2019 FEI # 1000220733
Zimmer Biomet, Inc.
Z-1739-2019 - Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420324Phase 3 Femoral Drill Guide Extra Large 2 06/06/2019 FEI # 1000220733
Zimmer Biomet, Inc.
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