Biomet, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2065-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill guide. The Oxford Fixed Bearing Knee is a Partial knee replacement system consisting of a femoral component and a fixed bearing tibial component for use in the lateral compartment of the knee. Partial replacement of the articulating surfaces of the knee when only one side of the knee joint is affected due to the compartmental primary degenerative or post-traumatic degenerative disease, previous tibial condyle or plateau fractures, deformity or revision of previous partial arthroplasty in the affected compartment. The Oxford Fixed Lateral bearings are indicated for use in the lateral compartment and intended to be implemented with bone cement.

Product Classification:

Class II

Date Initiated: June 3, 2015

Date Posted: July 22, 2015

Recall Number: Z-2065-2015

Event ID: 71529

Reason for Recall:

Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized diameter that can cause an interference with PN: 32-422822, Oxford Microplasty IM Link.

Status: Terminated

Product Quantity: 18

Code Information:

Part Number: 32-423400 Lot Numbers: 238220, 664720,489620, 490930,021410, 507150

Distribution Pattern:

Worldwide Distribution - US Nationwide in the states of NC, IN, PA, OH and the country of the Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated