Class II — Advanced Research Medical, LLC
| Recalling firm | ADVANCED RESEARCH MEDICAL, LLC |
|---|---|
| Registered facility | ADVANCED RESEARCH MEDICAL (the firm's only registered facility) |
| Classification | Class II |
| Status | Completed |
| Reason | 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 |
| Quantity | 1150 units |
| Distribution | US Nationwide distribution in the state of Minnesota. |
| Initiated | 2023-03-14 |
| Classified | 2024-04-29 |
| Recall number | Z-1698-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Advanced Research Medical, LLC (Z-1698-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94279/
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