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

Recall Z-1821-2024 — APTUS 2.8 TriLock Screw 22mm, HD7, 1/Pkg. Metal bone fixation fastener used with the APTUS fixation system.

U.S. FDA — Device Enforcement · United States · 2024-04-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1821-2024
Date of alert
2024-04-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medartis Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
24377397
Reported risk: Screw is 16mm long instead of 22mm long.
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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