Device recall
Z-1236-06: GORE TAG THORACIC ENDOPROSTHESIS System, Endovascular Graft, Aortic Aneurysm…
FDA device recall · Class II · W L Gore & Assoc, Inc.
Key facts
| Recall number (Z-number) | Z-1236-06 |
|---|---|
| Recall event | 35507 |
| Product | GORE TAG THORACIC ENDOPROSTHESIS System, Endovascular Graft, Aortic Aneurysm Treatment, Catalogue Number TG3410, 34mm x 10cm |
| Product code | MIH |
| Recalling firm | W L Gore & Assoc, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2006 |
| PMA numbers | P040043 |
| FEI number | 2017233 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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