Manufacturer

Biomet U.K., Ltd.

26 recalls in our database name Biomet U.K., Ltd. as the manufacturing or recalling firm.

What the numbers show

Total: 26
Critical: 0
Severe: 3
Most recent: 2017-03-01

Of the 26 recalls from Biomet U.K., Ltd. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3 (12%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–25 of 26

SevereFDA (Devices)·Z-1165-2017·2017-03-01
Biomet Recalls Oxford Partial Knee Trial Trays Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System trial trays due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee System Left Medial Tibial Trial Tray Size C
Category
Medical Device
Distribution
14 states
SevereFDA (Devices)·Z-1164-2017·2017-03-01
Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
SevereFDA (Devices)·Z-1167-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1152-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee System Tibial Resector Body Tubes and Guides due to potential alumina inclusions that could cause the instruments to crack or separate.
Product
Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1155-2017·2017-03-01
Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1153-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System Femoral Slap Hammers due to potential alumina inclusions that could cause the instruments to crack or separate.
Product
Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1161-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1156-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K. is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1175-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1159-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1154-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1173-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1174-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1158-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1166-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1162-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1169-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1157-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1170-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 1 instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1171-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1163-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1168-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 3 instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1160-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1172-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1124-2013·2013-04-24
Biomet Oxford Uni Knee System Toffee Hammer Recalled for Weld Cracking
Biomet U.K., Ltd. is recalling 430 Oxford Uni Knee System Toffee Hammers because excessive use may cause the head to detach from the handle.
Product
REF 32-422760 Oxford Uni Knee System,Toffee Hammer, non-sterile, found in REF 32-422763 Oxford Mlcroplasty Knee System Tibial instrument Tray small surgical hammer supplied with the Oxford Partial Knee Microplasty Instrument set, used for impacting implants.
Category
Medical Device
Distribution
Distributed nationwide