Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the blister pack may be...
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
Stryker End Cap, Standard T2 Humerus ¿6 mm Catalog Number: 18300003S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.
Quantity: 109 OUS
Why Was This Recalled?
Seal integrity of the blister pack may be compromised and sterility cannot be assured
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