Device recall
Z-0469-06: AngioJet XMI Rapid Exchange +, 4F, 135 cm. Contents: One (1) Thrombectomy…
FDA device recall · Class III · Possis Medical, Inc
Key facts
| Recall number (Z-number) | Z-0469-06 |
|---|---|
| Recall event | 34214 |
| Product | AngioJet XMI Rapid Exchange +, 4F, 135 cm. Contents: One (1) Thrombectomy Catheter for Peripheral Use. Sterilized with Ethylene Oxide. Single Use Only. Manufactured and Distributed by: Possis Medical, Inc. 9055 Evergreen Boulevard NW, Minneapolis, MN 55433-8003 USA. |
| Product code | DXE |
| Recalling firm | Possis Medical, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 8, 2006 |
| 510(k) numbers | K042874 |
| 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