Device recall
Z-1683-2017: Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts…
FDA device recall · Class II · National Biological Corp
Key facts
| Recall number (Z-number) | Z-1683-2017 |
|---|---|
| Recall event | 76725 |
| Product | Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototherapy treatment. |
| Product code | FTC |
| Recalling firm | National Biological Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 8, 2019 |
| 510(k) numbers | K872604 |
| 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