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 The manufacturer has discovered that potentially out-of-specification products...
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, A/R T2 Femur ¿12x360 mm, Product Number 18251236S
Quantity: 9
Why Was This Recalled?
The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.
Where Was This Sold?
This product was distributed to 7 states: AL, FL, KY, NC, TN, UT, WA
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