Device recall
Z-1090-06: Duraflo Treated Aortic Perfusion Cannula with plastic tip, 22 Fr. x 28 cm…
FDA device recall · Class II · Edwards Lifesciences Research Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1090-06 |
|---|---|
| Recall event | 35291 |
| Product | Duraflo Treated Aortic Perfusion Cannula with plastic tip, 22 Fr. x 28 cm., Edwards Lifesciences |
| Product code | DWF |
| Recalling firm | Edwards Lifesciences Research Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 11, 2008 |
| 510(k) numbers | K831769 |
| FEI number | 1713910 |
At a glance
- 1–9 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