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

Recall Z-1622-2024 — TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D

U.S. FDA — Device Enforcement · United States · 2024-02-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1622-2024
Date of alert
2024-02-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Howmedica Osteonics Corp.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
07613327380903
Reported risk: The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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