Device recall
Z-2635-2014: SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the…
FDA device recall · Class II · JK Products & Services, Inc
Key facts
| Recall number (Z-number) | Z-2635-2014 |
|---|---|
| Recall event | 69038 |
| Product | SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin. |
| Product code | LEJ |
| Recalling firm | JK Products & Services, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2017 |
| 510(k) numbers | K932483 |
| FEI number | 2311923 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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