Device recall
Z-1309-2008: HOUVA III Phototherapy System with DermaSense Technology comes on one skid…
FDA device recall · Class III · National Biological Corp
Key facts
| Recall number (Z-number) | Z-1309-2008 |
|---|---|
| Recall event | 46834 |
| Product | HOUVA III Phototherapy System with DermaSense Technology comes on one skid within 10 cardboard boxes. A therapeutic product designed for individuals who require specific Ultraviolet radiation therapy for diagnosed skin disorders. |
| Product code | FTC |
| Recalling firm | National Biological Corp |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 20, 2011 |
| 510(k) numbers | K041212 |
| FEI number | 1521608 |
At a glance
- 1–9 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