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

Recall Z-1791-2024 — TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx Only

U.S. FDA — Device Enforcement · United States · 2024-03-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1791-2024
Date of alert
2024-03-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
TriMed Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00842188127878
Reported risk: Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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