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Recall company profile

Biomet U.K., Ltd. Recalls

Overview of recall records associated with Biomet U.K., Ltd., including dates, categories and classifications where available.

24recall records

Mar 1, 2017latest record date

Mar 1, 2017earliest record date

Recall history in this database

Classification mix: Class II: 24.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage recall — FDA Z-1161-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Product Usage recall — FDA Z-1164-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Right Medial Tibial Trial Tray Size F Product Usage recall — FDA Z-1156-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size B Product recall — FDA Z-1175-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage recall — FDA Z-1160-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product recall — FDA Z-1171-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use recall — FDA Z-1153-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Left Medial Tibial Trial Tray Size B Product Usage recall — FDA Z-1167-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage recall — FDA Z-1157-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product recall — FDA Z-1172-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage recall — FDA Z-1159-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial recall — FDA Z-1165-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for recall — FDA Z-1168-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for recall — FDA Z-1170-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments recall — FDA Z-1154-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product recall — FDA Z-1173-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size B Product recall — FDA Z-1174-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Left Medial Tibial Trial Tray Size D Product Usage recall — FDA Z-1163-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Right Medial Tibial Trial Tray Size A Product Usage recall — FDA Z-1158-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Right Medial Tibial Trial Tray Size B Product Usage recall — FDA Z-1166-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Product recall — FDA Z-1155-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Partial Knee System Right Medial Tibial Trial Tray Size D Product Usage recall — FDA Z-1162-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments recall — FDA Z-1152-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Medical DeviceMar 1, 2017

Biomet U.K Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Instruments for recall — FDA Z-1169-2017

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 produce the…

Class IIFDA: TerminatedBiomet U.K., Ltd.

Understanding this recall history

This page summarizes recall records in which the official source identifies Biomet U.K., Ltd. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.