Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker CinchLock Flex Knotless Anchor with Inserter and Suture Recalled by Stryker Corporation Due to Increase in complaints concerning "pullwire" breakage that may...
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 Corporation directly.
Affected Products
Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197
Quantity: 9521 units
Why Was This Recalled?
Increase in complaints concerning "pullwire" breakage that may result in the broken pullwire remaining in the anchor implant body after deployment.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Corporation
Stryker Corporation has 108 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report