Device recall
Z-2636-2023: ProSun International Luxura Vegaz, Model 52X; Ultraviolet Tanning Device
FDA device recall · Class II · J&T Health and Wellness LLC
Key facts
| Recall number (Z-number) | Z-2636-2023 |
|---|---|
| Recall event | 92217 |
| Product | ProSun International Luxura Vegaz, Model 52X; Ultraviolet Tanning Device |
| Product code | LEJ |
| Recalling firm | J&T Health and Wellness LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000525872 |
At a glance
- None 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