Advanced Research Medical, LLC: Medical Device Recall in 2024 - (Recall #: Z-1698-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 14, 2023

Date Posted: May 8, 2024

Recall Number: Z-1698-2024

Event ID: 94279

Reason for Recall:

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

Status: Completed

Product Quantity: 1150 units

Code Information:

UDI/DI 00850014575311, Lot Numbers: 87458, BB059AA, BB140AA, BB140AB, BB307AA, BB350AA, BC061AA, BC130AA, BC130AA-2, BC274AA, BD083AA, BD083AB, BD083AC

Distribution Pattern:

US Nationwide distribution in the state of Minnesota.

Voluntary or Mandated:

Voluntary: Firm initiated