MicroAire Surgical Instruments, LLC recalls MicroAire SmartRelease Endoscopic System, Endoscopic Carpal Tunnel Release, SmartRelease Handpiece, containing IFU rev.

Recalled June 13, 2018 · FDA recall Z-2107-2018 · MicroAire Surgical Instruments

Hazard

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

Units

2009

Sold at

Worldwide Distribution - USA (nationwide) including Puerto Rico and to the countries of: Australia, Belgium, Brazil, Canada, Chile, Czech Republic, Denmark, France, Germany, Hong Kong, India, Iran, Ireland, Israel, Italy, Jordan, Korea, Lebanon, Mexico, Nicaragua, Poland, Russia, Saudi Arabia, Serbia, Singapore, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, UAE, and UK.

Description

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

Product

MicroAire SmartRelease Endoscopic System, Endoscopic Carpal Tunnel Release, SmartRelease Handpiece, containing IFU rev. D The MicroAire Carpal Tunnel Release System is for use in patients diagnosed with carpal tunnel syndrome that is not associated with, or secondary to, any other known pathology (i.e., idiopathic carpal tunnel syndrome). Preoperative x-rays of the wrist, including a carpal tunnel view, are recommended to aid in the diagnosis of associated pathology (i.e., calcific tendonitis, fracture of the hook of the hamate). This device is indicated for releasing the transverse carpal ligament (flexor retinaculum).

Manufacturer(s)

MicroAire Surgical Instruments, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →