Device recall
Z-0157-2007: The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP…
FDA device recall · Class III · St. Jude Medical / Daig Division
Key facts
| Recall number (Z-number) | Z-0157-2007 |
|---|---|
| Recall event | 35819 |
| Product | The affected device is labeled Angio-Seal Vascular Closure Device 6F VIP Platform, model 610130. The recalled product is the 6 French model size. |
| Product code | MGB |
| Recalling firm | St. Jude Medical / Daig Division |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 13, 2006 |
| PMA numbers | P930038, P930038S040 |
| FEI number | 2182269 |
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