Device recall
Z-1048-2017: AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75 V…
FDA device recall · Class II · Endologix
Key facts
| Recall number (Z-number) | Z-1048-2017 |
|---|---|
| Recall event | 76256 |
| Product | AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75 V F0070308 A2828/C75 V F0070312 A3434/C80 V f00553 I1616/C55F SA F00556 I2013/C70F SA F00555 I2020/C55F SA F00558 IS2025/C55 SA F00559 IS2025/C65 SA F0072605 A2525/C75O20 V F0072606 A2525/C95O20 V f00552 I1616/C88 SA F00557… |
| Product code | MIH |
| Recalling firm | Endologix |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2017 |
| PMA numbers | P040002 |
| FEI number | 3011063223 |
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