Device recall
Z-1675-2013: AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables…
FDA device recall · Class II · Angiodynamics, INC
Key facts
| Recall number (Z-number) | Z-1675-2013 |
|---|---|
| Recall event | 65439 |
| Product | AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables are indicated for use with the RITA RF Generators and RITA electrosurgical devices. |
| Product code | GEI |
| Recalling firm | Angiodynamics, INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 12, 2015 |
| 510(k) numbers | K040989 |
| 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