Device recall
Z-0149-2008: Vortex VX, Port System, 9.6FR, REF/Part Number: P5455K, Catalog Number: P5455…
FDA device recall · Class II · Rita Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0149-2008 |
|---|---|
| Recall event | 45404 |
| Product | Vortex VX, Port System, 9.6FR, REF/Part Number : P5455K, Catalog Number: P5455, Latex Free, Sterile, AngioDynamics Incorporated, Manchester, GA. 31816 |
| Product code | LJT |
| Recalling firm | Rita Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 14, 2008 |
| 510(k) numbers | K010189 |
| FEI number | 3017892510 |
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