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MicroAire Surgical Instruments, LLC recalls MicroAire K-Wires
Recalled March 15, 2017 · FDA recall Z-1407-2017 · MicroAire Surgical Instruments
Hazard
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). · FDA Class II
Units
Total 362
Sold at
United States.
Description
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).
Product
MicroAire K-Wires
Manufacturer(s)
MicroAire Surgical Instruments, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →