Device recall
Z-1816-2008: ev3 The Endovascular Company, IntraCoil Self-Expanding Peripheral Stent, Model…
FDA device recall · Class III · Ev3, Inc
Key facts
| Recall number (Z-number) | Z-1816-2008 |
|---|---|
| Recall event | 48102 |
| Product | ev3 The Endovascular Company, IntraCoil Self-Expanding Peripheral Stent, Model REF VT-6-60-135, Lot 4401214, Use Before 2010-07. |
| Product code | NIP |
| Recalling firm | Ev3, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 27, 2009 |
| PMA numbers | P000033 |
| FEI number | 2183870 |
At a glance
- None 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