Device recall
Z-1762-2025: Tornado Embolization Microcoil, intended for embolization of selective vessel…
FDA device recall · Class II · Cook Incorporated
Key facts
| Recall number (Z-number) | Z-1762-2025 |
|---|---|
| Recall event | 96702 |
| Product | Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular lesions, RPN MWCE-18S-3/2-TORNADO (GPN G08261), RPN MWCE-18S-3/2-TORNADO-081800 (GPN G13102), RPN MWCE-18S-4/2-TORNADO (GPN G08357) |
| Product code | KRD |
| Recalling firm | Cook Incorporated |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1820334 |
At a glance
- None 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