Advanced Research Medical, LLC recalls ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop Blade, Part # 01-06-4; treatment

Recalled May 8, 2024 · FDA recall Z-1698-2024 · Advanced Research Medical

Hazard

Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Assembly during surgery. · FDA Class II

Units

1150 units

Sold at

US Nationwide distribution in the state of Minnesota.

Description

Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Assembly during surgery.

Product

ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop Blade, Part # 01-06-4; treatment of degenerative disc disease

Manufacturer(s)

Advanced Research Medical, LLC

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