Device recall
Z-1131-2007: Possis AngioJet XVG Thrombectomy Sets, Model/Order # 105042-001, Sterilized with…
FDA device recall · Class II · Possis Medical, Inc
Key facts
| Recall number (Z-number) | Z-1131-2007 |
|---|---|
| Recall event | 38244 |
| Product | Possis AngioJet XVG Thrombectomy Sets, Model/Order # 105042-001, Sterilized with Ethylene Oxide, Possis Medical, Inc., 9055 Evergreen Boulevard NW, Minneapolis, MN 55433-8003. (These sets are used with the new AngioJet Ultra Console) |
| Product code | DXE |
| Recalling firm | Possis Medical, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 2, 2008 |
| 510(k) numbers | K050794 |
| FEI number | 2183460 |
At a glance
- 1–9 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