Biomet, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1018-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Oxford Partial Knee System, Fixed Lateral Tibial Construct- Intended to replace part of a knee joint when used in conjunction with a femoral and tibial component Item Number: 154341

Product Classification:

Class II

Date Initiated: December 15, 2022

Date Posted: February 1, 2023

Recall Number: Z-1018-2023

Event ID: 91365

Reason for Recall:

Packaged in the incorrect shelf carton. Incorrect shelf carton; outer carton is smaller than the required outer carton, which forces the Tyvex pouch to be folded and packaged in the carton causing compound creases and compromise the sterile barrier

Status: Ongoing

Product Quantity: 7 units

Code Information:

UDI: (01) 05019279515349 (17) 241123 (10) 077830 Lot Number: 077830

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states of IN, KY and the countries of Canada, New Zealand, Japan, Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated