Device recall
Z-1095-06: Aortic Perfusion Cannula with Metal Tip, 22 Fr. x 23 cm., Edwards Lifesciences
FDA device recall · Class II · Edwards Lifesciences Research Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1095-06 |
|---|---|
| Recall event | 35291 |
| Product | Aortic Perfusion Cannula with Metal Tip, 22 Fr. x 23 cm., Edwards Lifesciences |
| Product code | DWF |
| Recalling firm | Edwards Lifesciences Research Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 11, 2008 |
| FEI number | 1713910 |
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