# FDA recall Z-1698-2024

> **Advanced Research Medical, LLC** · Class II · device recall initiated 2023-03-14.

## Product

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

## 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.

## Key facts

- **Recall number:** Z-1698-2024
- **Recalling firm:** Advanced Research Medical, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2023-03-14
- **Report date:** 2024-05-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Burnsville, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1698-2024

## Citation

> AI Analytics. FDA recall Z-1698-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1698-2024. Source: US FDA. Licensed CC0.

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