MicroAire Surgical Instruments

14 recalls β€’ β€’ Categories: Other Medical Devices, Infusion Pumps, Implants & Prosthetics

The Instructions for Use (IFU) is incorrect with regards to sterilization parameters and must be replaced.

Apr 19, 2018 Infusion Pumps Nationwide View Details β†’
Class I - Dangerous

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).

Feb 21, 2017 Other Medical Devices View Details β†’

MicroAire has initiated a limited recall (29 Units)on the Endotine Transbleph 3.5 (CFD-080-0167), Lot # 285373, due to minor mislabeling ( the front label is correct, but the side label lists an incorrect part number, i.e. CFD-080-0177).

May 6, 2016 Other Medical Devices View Details β†’

A medical device used in surgical procedures was packaged in a pouch in which a defective seal may compromise sterility

Aug 12, 2013 Implants & Prosthetics Nationwide View Details β†’

A medical device used in surgical procedures was packaged in a pouch in which a defective seal may compromise sterility

Aug 12, 2013 Implants & Prosthetics Nationwide View Details β†’