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

Recall Z-1039-2025 — NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10

U.S. FDA — Device Enforcement · United States · 2025-01-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1039-2025
Date of alert
2025-01-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00889024635746
Reported risk: It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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