Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arthrex Suture Anchor Recalled by Arthrex, Inc. Due to Potentially lead to anchor breakage during insertion,
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 Arthrex, Inc. directly.
Affected Products
Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with needles.) Part Number AR-1317FT Product Usage: Soft tissue fixation to bone in the hand and wrist
Quantity: 1308 US and 110 OUS
Why Was This Recalled?
Potentially lead to anchor breakage during insertion,
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Arthrex, Inc.
Arthrex, Inc. has 28 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report