Device recall
Z-2337-2018: Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135
FDA device recall · Class II · Terumo Medical Corp
Key facts
| Recall number (Z-number) | Z-2337-2018 |
|---|---|
| Recall event | 80242 |
| Product | Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135 |
| Product code | MGB |
| Recalling firm | Terumo Medical Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2019 |
| PMA numbers | P930038 |
| FEI number | 2243441 |
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