MicroAire Surgical Instruments, LLC: Medical Device Recall in 2017 - (Recall #: Z-1407-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

MicroAire K-Wires

Product Classification:

Class II

Date Initiated: February 21, 2017

Date Posted: March 15, 2017

Recall Number: Z-1407-2017

Event ID: 76560

Reason for Recall:

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).

Status: Terminated

Product Quantity: Total 362

Code Information:

Part Number, Lot Number, Quantity Distributed to Field 1600-9355NS, 61005, 56; 1600-9625NS, 60297, 209; 1604-162NS, 62856, 97.

Distribution Pattern:

United States.

Voluntary or Mandated:

Voluntary: Firm initiated