Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
K-Wire Recalled by Arthrex, Inc. Due to Products do not meet length and diameter specifications.
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
K-Wire, 1.35 mm x 170 mm
Quantity: 300 pieces
Why Was This Recalled?
Products do not meet length and diameter specifications.
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