Biomet Recalls Oxford Fixed Bearing Partial Knee Components
Biomet is recalling 25 Oxford Fixed Bearing Partial Knee components due to a design defect that may cause anterior impingement between bone and the poly bearing.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device with a design defect that creates a potential for injury (anterior impingement), but the source text does not report any actual injuries or illnesses, fitting the criteria for a risk-of-harm product where injury has not yet been reported.
Plain-English summary
Biomet, Inc. is recalling 25 units of the REF 154207 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia, Size B3. These medical devices are partial knee replacement systems consisting of a femoral component and a fixed bearing tibial component intended for use in the lateral compartment of the knee with bone cement.
The recall was initiated after a Biomet investigation found that the design of the tibial bearing creates the potential for anterior impingement between the bone and the poly bearing component in terminal extension. The affected units were distributed worldwide, including in the United States (North Carolina, Indiana, Pennsylvania, and Ohio), Canada, and the Netherlands.
Healthcare providers and patients who have received these specific components should contact Biomet, Inc. for further instructions on how to proceed. The recall number for this action is Z-1700-2013.
The recalled product
- Product
- REF 154207 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size B3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartment Sterile R The Oxford Fixed Bearing Knee is a Partial knee replacement system consisting of a femoral component and a fixed bearing
- Manufacturer
- Biomet, Inc.
- Hazard
- Affected units
- 25
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- M561220 M584370 M151880
- M444690
- M886370
- M956050
Distribution
Part of a larger recall action
This product is one of 30 recalled by Biomet, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 30 products in this recall →Related recalls
Same manufacturer · Biomet, Inc.
See all →- ModerateIntramedullary Bone Saw Blade Assembly Recalled Due to Potential Packaging Damage
FDA (Devices) · 2026-08-12
- HighIntramedullary Bone Saw Blade Assembly Recalled Due to Potential Sterile Barrier Damage
FDA (Devices) · 2026-08-12
- HighIntramedullary Bone Saw Blade Assembly Recall for Packaging Damage
FDA (Devices) · 2026-08-12
- ModerateIntramedullary Bone Saw Blade Assembly Recalled Due to Potential Sterile Barrier Damage
FDA (Devices) · 2026-08-12
- HighIntramedullary Bone Saw Blade Assemblies Recalled Due to Potential Packaging Damage
FDA (Devices) · 2026-08-12
Same hazard · design defect
See all →- HighUnited Orthopedic Recalls U2 Total Knee System Femoral Offset Bushings
FDA (Devices) · 2026-08-12
- SevereBioFlo DuraMax catheters recalled as Class I over sheath introducer defect
FDA (Devices) · 2026-04-01
- SevereProGuide chronic dialysis catheters recalled as Class I over sheath introducer defect
FDA (Devices) · 2026-04-01
- SevereDuraMax hemodialysis catheter sheath introducer may not split as intended
FDA (Devices) · 2026-04-01
- SevereMerit 16F splittable sheath introducer recalled as Class I bulk product
FDA (Devices) · 2026-04-01