Device recall
Z-0503-2007: Alsius Cool Line Catheter, Model CL-2295AE
FDA device recall · Class II · Alsius Corporation
Key facts
| Recall number (Z-number) | Z-0503-2007 |
|---|---|
| Recall event | 37192 |
| Product | Alsius Cool Line Catheter, Model CL-2295AE |
| Product code | NCX |
| Recalling firm | Alsius Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 22, 2007 |
| 510(k) numbers | K014241 |
| FEI number | 3002922896 |
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