Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Suture Anchor Recalled by Arthrex, Inc. Due to Not properly sterilized, because the outer pouch seal...
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
Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, Closed Eyelet, REF AR-2323BCC
Quantity: 3985 pieces
Why Was This Recalled?
Not properly sterilized, because the outer pouch seal on the Tyvek header was sealed closely to the foil pouch.
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