Device recall
Z-0092-04: Solar 8000M Patient Monitor with software versions 3A, 3B and 3C
FDA device recall · Class II · General Electric Medical Systems Information Technology
Key facts
| Recall number (Z-number) | Z-0092-04 |
|---|---|
| Recall event | 27558 |
| Product | Solar 8000M Patient Monitor with software versions 3A, 3B and 3C |
| Product code | DSI |
| Recalling firm | General Electric Medical Systems Information Technology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 8, 2005 |
| FEI number | 2124823 |
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