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

Recall Z-1011-2018 — Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty

U.S. FDA — Device Enforcement · United States · 2017-10-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1011-2018
Date of alert
2017-10-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0088030427068
Reported risk: The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur.
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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