Device recall
Z-0677-06: Angio-Seal Vascular Closure Device. Ref 610109. 6F STS Platform. Sterilized by…
FDA device recall · Class II · St. Jude Medical / Daig Division
Key facts
| Recall number (Z-number) | Z-0677-06 |
|---|---|
| Recall event | 33329 |
| Product | Angio-Seal Vascular Closure Device. Ref 610109. 6F STS Platform. Sterilized by gamma radiation. For single use only. St. Jude Medical, Daig Division, Inc., Minnetonka, MN 55345-2126, USA. |
| Product code | MGB |
| Recalling firm | St. Jude Medical / Daig Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 22, 2006 |
| PMA numbers | P930038 |
| 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