Device recall
Z-0592-2008: Hoana LifeBed Patient Vigilance System, (Intelligent Medical Vigilance…
FDA device recall · Class II · Hoana Medical
Key facts
| Recall number (Z-number) | Z-0592-2008 |
|---|---|
| Recall event | 46154 |
| Product | Hoana LifeBed Patient Vigilance System, (Intelligent Medical Vigilance System),Model Number: 010135-01, Product distributed by Hoana Medical, Inc., 828 Fort St. Mall, Suite 620, Honolulu, HI |
| Product code | KMI |
| Recalling firm | Hoana Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 1, 2008 |
| FEI number | 3005596882 |
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