Device recall
Z-1472-2009: Arrow Embolectomy Catheters: 5 French, 2 Lumen x 80cm, Product Number: W01801…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-1472-2009 |
|---|---|
| Recall event | 51960 |
| Product | Arrow Embolectomy Catheters: 5 French, 2 Lumen x 80cm, Product Number: W01801, Single use, Latex Free, Rx only, Arrow International, 2400 Bernville Road, Reading, PA 19605. The arterial embolectomy catheter is intended for use in removing arterial emboli. |
| Product code | DXE |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 1, 2010 |
| 510(k) numbers | K902327 |
| FEI number | 3015859709 |
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