Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MicroAire K-Wires Recalled by MicroAire Surgical Instruments, LLC Due to Mislabeling
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 MicroAire Surgical Instruments, LLC directly.
Affected Products
MicroAire K-Wires
Quantity: Total 362
Why Was This Recalled?
Mislabeling on three lots of K-Wires. The incorrect product description " dual trocar" instead of "single trocar" was on the product label on the following parts: 1600-9355NS (lot 61005), 1600-9625NS (lot 60297), and 1604-162NS (lot 62856).
Where Was This Sold?
United States.
About MicroAire Surgical Instruments, LLC
MicroAire Surgical Instruments, LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report