Device recall
Z-1698-2024: ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible…
FDA device recall · Class II · Advanced Research Medical, LLC
Key facts
| Recall number (Z-number) | Z-1698-2024 |
|---|---|
| Recall event | 94279 |
| Product | ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop Blade, Part # 01-06-4; treatment of degenerative disc disease |
| Product code | MAX |
| Recalling firm | Advanced Research Medical, LLC |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K173947 |
| FEI number | 3016002322 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database