Device recall
Z-1550-2013: IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent…
FDA device recall · Class II · IDEV Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-1550-2013 |
|---|---|
| Recall event | 65245 |
| Product | IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms |
| Product code | FGE |
| Recalling firm | IDEV Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 29, 2013 |
| 510(k) numbers | K111766 |
| FEI number | 3005325609 |
At a glance
- 1–9 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