Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1036-2023 — 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

U.S. FDA — Device Enforcement · United States · 2022-11-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1036-2023
Date of alert
2022-11-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00880304082991
Reported risk: Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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