Device recall
Z-0309-2007: Endologix Infrarenal Bifurcated Powerlink System with Visifiex Delivery System…
FDA device recall · Class II · Endologix Inc
Key facts
| Recall number (Z-number) | Z-0309-2007 |
|---|---|
| Recall event | 36803 |
| Product | Endologix Infrarenal Bifurcated Powerlink System with Visifiex Delivery System (endovascular graft). Model Number 25-16-155BL |
| Product code | MIH |
| Recalling firm | Endologix Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 4, 2011 |
| PMA numbers | P040042 |
| FEI number | 1000125107 |
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