Device recall
Z-0689-2008: Medtronic brand AneuRx AAAdvantage Endovascular Stent Graft with the Xcelerant…
FDA device recall · Class II · Medtronic CardioVascular
Key facts
| Recall number (Z-number) | Z-0689-2008 |
|---|---|
| Recall event | 46353 |
| Product | Medtronic brand AneuRx AAAdvantage Endovascular Stent Graft with the Xcelerant Delivery System; Model Numbers Affected: All AAAdvantage models including: AEXC202040, IEXC121255, ILXC1212115, ILXC151585, AEXC222240, IEXC131355, ILXC1212135, ILXC1616115, AEXC242440, IEXC141455, ILXC121285… |
| Product code | MIH |
| Recalling firm | Medtronic CardioVascular |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 28, 2008 |
| PMA numbers | P990020 |
| FEI number | 3001452571 |
At a glance
- None 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