Device recall
Z-1483-06: Cordis Neurovascular Pre-Shaped Prowler Select Infusion Catheters.
FDA device recall · Class II · Cordis Neurovascular, Inc.
Key facts
| Recall number (Z-number) | Z-1483-06 |
|---|---|
| Recall event | 36077 |
| Product | Cordis Neurovascular Pre-Shaped Prowler Select Infusion Catheters. |
| Product code | KRA |
| Recalling firm | Cordis Neurovascular, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 25, 2008 |
| 510(k) numbers | K021591 |
| FEI number | 1000222137 |
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