Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that one lot of the T2...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker GmbH directly.
Affected Products
Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
Quantity: 1
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker GmbH
Stryker GmbH has 68 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report