Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arthrex Deltoid Ligament Reconstruction Implant System. Intended as a fixation Recalled by Arthrex, Inc. Due to Potential for a component contained in the Implant...
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 Deltoid Ligament Reconstruction Implant System. Intended as a fixation post, a distribution bridge or for distributing suture tension over areas of ligament or tendon repair utilizing titanium buttons.
Quantity: 117 devices
Why Was This Recalled?
Potential for a component contained in the Implant System to be non-sterile.
Where Was This Sold?
This product was distributed to 22 states: AZ, AR, CA, CO, FL, IL, IN, KS, KY, LA, MD, MO, NV, NJ, NY, NC, OH, PA, SD, TN, TX, WI
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