Device recall
Z-2792-2011: Abbott Vascular COPILOT Kit, COPILOT Bleedback Control Valve Part Number…
FDA device recall · Class II · Abbott Vascular
Key facts
| Recall number (Z-number) | Z-2792-2011 |
|---|---|
| Recall event | 58979 |
| Product | Abbott Vascular COPILOT Kit, COPILOT Bleedback Control Valve Part Number : 1003330. For use in cardiac diagnostic or therapeutic procedures. |
| Product code | DTL |
| Recalling firm | Abbott Vascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 26, 2012 |
| 510(k) numbers | K991102 |
| FEI number | 2024168 |
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