Device recall
Z-1025-03: Vail Enclosed Bed System, model 1000
FDA device recall · Class II · Vail Products Inc
Key facts
| Recall number (Z-number) | Z-1025-03 |
|---|---|
| Recall event | 26504 |
| Product | Vail Enclosed Bed System, model 1000 |
| Product code | FNL |
| Recalling firm | Vail Products Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2008 |
| FEI number | 1000122546 |
At a glance
- None 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