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

Recall Z-0824-2015 — Bone Screw, self-tapping The Trilogy shells are available in three configurations; uni, multi, and cluster-holed. The multi and cluster-holed shells allow for the use of screws to provide additional fixation and security, particularly in those case where acetabular bone stock is deficient. The Tril

U.S. FDA — Device Enforcement · United States · 2014-11-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0824-2015
Date of alert
2014-11-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Manufacturing B.V.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
62748089
Reported risk: Analysis of returned complaint devices, product in inventory, and device manufacturing records has identified tool marks isolated to one specific machining mill to be the cause of the fractures. .
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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