Device recall
Z-2793-2011: Guidant RAPIDO Cut-Away Guiding Catheter, 6F. Part Numbers: 66676-201 and…
FDA device recall · Class II · Abbott Vascular
Key facts
| Recall number (Z-number) | Z-2793-2011 |
|---|---|
| Recall event | 58979 |
| Product | Guidant RAPIDO Cut-Away Guiding Catheter, 6F. Part Numbers: 66676-201 and 667552-100. For use in cardiac diagnostic and therapeutic procedures. |
| Product code | DQY |
| Recalling firm | Abbott Vascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 26, 2012 |
| 510(k) numbers | K021455, K031459, K031505, K031688, K031903 |
| FEI number | 2024168 |
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