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Oxford® Partial Knee System

Biomet Uk Ltd · Model 112211500 · UDI-DI 00889024683228

NRA Prescription
0
510(k) clearances
5,146
Adverse events (58 deaths)
32
Recalls
16
Facilities

Recalls

DateFirmReason
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro
2016-01-05Biomet U.K., Ltd.Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to pro

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.