Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Recalled by Arthrex, Inc. Due to There is a potential for blockage of the...
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 Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Quantity: 47
Why Was This Recalled?
There is a potential for blockage of the Hub Attachment Tube.
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