Device recall
Z-0707-05: Voyager RX Coronary Dilatation Catheter
FDA device recall · Class II · Guidant Corporation Advanced CardiovascularSystem
Key facts
| Recall number (Z-number) | Z-0707-05 |
|---|---|
| Recall event | 31116 |
| Product | Voyager RX Coronary Dilatation Catheter |
| Product code | MAF |
| Recalling firm | Guidant Corporation Advanced CardiovascularSystem |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 29, 2012 |
| PMA numbers | P810046, P810046S216 |
| FEI number | 2024168 |
At a glance
- None 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