Biomet, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1036-2023)

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:

OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee Item Number: CP260602

Product Classification:

Class II

Date Initiated: November 29, 2022

Date Posted: February 8, 2023

Recall Number: Z-1036-2023

Event ID: 91423

Reason for Recall:

Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement

Status: Ongoing

Product Quantity: 2 units

Code Information:

UDI: (01)00880304082991(17)321103(10)136620 Lot Number: 136620

Distribution Pattern:

US Nationwide distribution in the states of CA, KY, FL.

Voluntary or Mandated:

Voluntary: Firm initiated