ProSun International Luxura Vegaz — Class II medical device recall Z-2636-2023
Ongoing recall by J&T Health and Wellness LLC, reported 2023-10-04. In some cases the communication isolator installed in the Model 52X can cause a disturbance in the glass-filte
| Recall number | Z-2636-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Recalling firm | J&T Health and Wellness LLC, Saint Petersburg, FL, United States |
| Recall initiated | 2023-03-31 |
| Classified | 2023-09-28 |
| Reported by FDA | 2023-10-04 |
| Quantity | 12 units |
| Reason classes | foreign material |
| Model numbers | 52X |
Product
ProSun International Luxura Vegaz, Model 52X; Ultraviolet Tanning Device
Reason for recall
In some cases the communication isolator installed in the Model 52X can cause a disturbance in the glass-filter safety circuit.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2636-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.