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

Recall Z-0469-2018 — Affixus Hip Fracture Nail, RH 130 DEG 11MM X 400MM

U.S. FDA — Device Enforcement · United States · 2017-08-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0469-2018
Date of alert
2017-08-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
814511400
Reported risk: During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
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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