Device recall
Z-1008-04: Ultraview 1700 Monitor Model 90387.
FDA device recall · Class II · Spacelabs Medical Inc.
Key facts
| Recall number (Z-number) | Z-1008-04 |
|---|---|
| Recall event | 29038 |
| Product | Ultraview 1700 Monitor Model 90387. |
| Product code | DSI |
| Recalling firm | Spacelabs Medical Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 8, 2006 |
| FEI number | 3010157426 |
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