Device recall
Z-1427-2010: InterGard Knitted Collagen Coated Vascular prostheses, Catalog number: IGK1206…
FDA device recall · Class II · Intervascular S.A.S.
Key facts
| Recall number (Z-number) | Z-1427-2010 |
|---|---|
| Recall event | 54562 |
| Product | InterGard Knitted Collagen Coated Vascular prostheses, Catalog number: IGK1206. InterVascular SAS, France. Indicated for surgical repair, bypass or replacement of arteries in the treatment of aneurysmal and occlusive disease of the abdominal aorta, visceral arteries, and peripheral arteries. |
| Product code | DSY |
| Recalling firm | Intervascular S.A.S. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 27, 2010 |
| 510(k) numbers | K964625 |
| FEI number | 3002707083 |
At a glance
- 1–9 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