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

Recall Z-3164-2018 — Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 280 mm, Item Number: 814613280

U.S. FDA — Device Enforcement · United States · 2018-07-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3164-2018
Date of alert
2018-07-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
814613280
Reported risk: The set screw is not able to advance or reverse from the original position in the nail.
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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