Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor Recalled by Smith & Nephew, Inc. Endoscopy Division Due to Distal part of the anchor may break on...
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 Smith & Nephew, Inc. Endoscopy Division directly.
Affected Products
Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor with two #2 ULTRABRAID sutures (blue, blue-COBRAID) with Needles Product Usage: intended for use for the reattachment of soft tissue to bone Part Number: 72202618
Quantity: 913 units
Why Was This Recalled?
Distal part of the anchor may break on insertion into bone during surgery
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Smith & Nephew, Inc. Endoscopy Division
Smith & Nephew, Inc. Endoscopy Division has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report