FDAFebruary 21, 2017device

MicroAire K-Wires

Official recall recorded by the U.S. Food & Drug Administration.

The 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).

What to do

FDA enforcement status: Terminated

Brands named

microaire surgical instrumentsmicroairemicroaire surgical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
MicroAire K-Wires — Recall Details · AllClear