FDA Device recall Z-2636-2023
ProSun International Luxura Vegaz, Model 52X
- FDA Device
- Class II
- ongoing
- Published 2023-10-04
On 2023-10-04 the FDA classified a Class II recall of ProSun International Luxura Vegaz, Model 52X by J And T Health And Wellness, citing in some cases the communication isolator installed in the Model 52X can cause a disturbance in the glass-filter safety circuit.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2636-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-31 |
| Published | 2023-10-04 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | J And T Health And Wellness |
| Distribution | n/a |
Product
ProSun International Luxura Vegaz, Model 52X; Ultraviolet Tanning Device
Reason
In some cases the communication isolator installed in the Model 52X can cause a disturbance in the glass-filter safety circuit.
Identifiers
| code_info | 52X0012, 52X0013, 52X0014, 52X0024, 52X0029, 52X0030, 52X0031, 52X0032, 52X0033, 52X0034, 52X0036, 52X0037 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2636-2023%22
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