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

Recall Z-2090-2013 — Free Lock Femoral Hip Fixation System Compression Lag Screw . Several lengths (55 to 150 mm) and diameters (12.7 and 15. 8 mm). Item codes starting with 00-1181-05, 00-1181-10 and 00-1181-15. ZIMMER Compression Hip Screw, orthopedic implant.

U.S. FDA — Device Enforcement · United States · 2013-06-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2090-2013
Date of alert
2013-06-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
60621340
Reported risk: Single packaging configuration used for the VERSA-FX-II Femoral Fixation System failed the leak test compromising the sterility of the product.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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