Device recall
Z-0894-06: Amplatz Goose Neck Microsnare Kit, Model SK400 (175 cm length x 4mm loop snare x…
FDA device recall · Class III · Ev3, Inc
Key facts
| Recall number (Z-number) | Z-0894-06 |
|---|---|
| Recall event | 34337 |
| Product | Amplatz Goose Neck Microsnare Kit, Model SK400 (175 cm length x 4mm loop snare x .018'',0.46mm) and SK701 (200 cm length x 7mm loop snare x 0.18'' x 0.46mm) ev3, 4600 Nathan Lane North, Plymouth, Minnesota, 55442-2920 USA. For one time use only. Sterilization with Ethylene Oxide gas. Do not… |
| Product code | DXE |
| Recalling firm | Ev3, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 26, 2006 |
| 510(k) numbers | K901502 |
| FEI number | 2183870 |
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