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

Recall Z-0291-2019 — Hoffman LRF Hexapod Strut, Extra Short 183mm-295mm, Model Number 4935-0-040. Product Usage - The Hoffmann LRF System is indicated in pediatric patients and adults for the treatment and fixation of: Open and closed fractures Post-traumatic joint contracture which has resulted in loss of range of

U.S. FDA — Device Enforcement · Switzerland · 2018-08-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0291-2019
Date of alert
2018-08-28
Country / jurisdiction
Switzerland
Risk level
Class II
Risk type
recall
Brand
Stryker GmbH
Product category
device
Product type
Devices
Reported risk: The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a reduced press fit of the pin. This can result in partial of full displacement or loss of the pin and, accordingly, stability of the strut of the frame cannot be ensured.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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