Device recall
Z-1918-2008: AneuRx AAAdvantage stent graft and the Xcelerant Delivery System with Hydro…
FDA device recall · Class II · Medtronic CardioVascular
Key facts
| Recall number (Z-number) | Z-1918-2008 |
|---|---|
| Recall event | 48097 |
| Product | AneuRx AAAdvantage stent graft and the Xcelerant Delivery System with Hydro, Product number ILXCH161685, manufactured by Medtronic Cardiovascular, Santa Rosa, CA. The product is designed to treat infrarenal abdominal aortic or aorto-iliac aneurysms during an endovascular approach. |
| Recalling firm | Medtronic CardioVascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 11, 2008 |
| PMA numbers | P990020 |
| FEI number | 3001452571 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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