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

Recall Z-0594-2020 — Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660

U.S. FDA — Device Enforcement · United States · 2019-10-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0594-2020
Date of alert
2019-10-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00880304386570
Reported risk: Possible commingle of 13 MM and 14 MM Intramedullary Bone Saw Cam Assembly -an Intramedullary Bone Saw Cam Assembly was labeled and etched as a 14 MM but measured as a 13 MM cam
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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