Device recall
Z-2587-2024: ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use…
FDA device recall · Class I · Inari Medical - Oak Canyon
Key facts
| Recall number (Z-number) | Z-2587-2024 |
|---|---|
| Recall event | 95069 |
| Product | ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-01011 |
| Product code | QEW |
| Recalling firm | Inari Medical - Oak Canyon |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K223210 |
| FEI number | 3020347218 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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