Device recall
Z-1076-04: Dispersive Electrodes packaged in an 8x10 plastic container.
FDA device recall · Class II · Rita Medical Systems
Key facts
| Recall number (Z-number) | Z-1076-04 |
|---|---|
| Recall event | 29383 |
| Product | Dispersive Electrodes packaged in an 8x10 plastic container. |
| Product code | JOS |
| Recalling firm | Rita Medical Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 25, 2004 |
| FEI number | 1000523114 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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