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

Recall Z-1939-2025 — Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.

U.S. FDA — Device Enforcement · Switzerland · 2025-05-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1939-2025
Date of alert
2025-05-22
Country / jurisdiction
Switzerland
Risk level
Class II
Risk type
recall
Brand
Stryker GmbH
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04546540646293
Reported risk: Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.
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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