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

Recall Z-0851-2015 — NexGen Complete Knee Solution Monoblock Tibial Provisional / Drill Guide Tibial Size 5 Femoral Size Green / CH Zimmer U.K. Ltd., SN3 4FP, UK Zimmer Trabecular Metal Technology, Inc 10 Pomeroy Road, Parsippany, NJ 07054 USA

U.S. FDA — Device Enforcement · United States · 2014-12-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0851-2015
Date of alert
2014-12-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Trabecular Metal Technology, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
62592928
Reported risk: During cleaning, two separate units of the NexGen Tibial Base plates did not fit with the Tibial Base Plate handle.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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