ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System — Class II medical device recall Z-1698-2024
Completed recall by Advanced Research Medical, LLC, reported 2024-05-08, distributed nationwide. Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Ass
| Recall number | Z-1698-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advanced Research Medical, LLC, Burnsville, MN, United States |
| Recall initiated | 2023-03-14 |
| Classified | 2024-04-29 |
| Reported by FDA | 2024-05-08 |
| Distributed | Nationwide (US) |
| Quantity | 1,150 units |
| UPC / GTIN / UDI-DI | 00850014575311 |
| Lot numbers | 87458, BB059AA, BB140AA, BB140AB, BB307AA, BB350AA, BC061AA, BC130AA, BC130AA-2, BC274AA, BD083AA, BD083AB, BD083AC |
| Model numbers | 01-06-4 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1698-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.