Class II

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

Advanced Research Medical, LLC · March 14, 2023

Reason for Recall

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

Distribution

US Nationwide distribution in the state of Minnesota.

States Affected

NATIONWIDE

Quantity Affected

1150 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1698-2024

Status: completed

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.