# FDA recall Z-2636-2023

> **J&T Health and Wellness LLC** · Class II · device recall initiated 2023-03-31.

## 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.

## Distribution

US

## Key facts

- **Recall number:** Z-2636-2023
- **Recalling firm:** J&T Health and Wellness LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-31
- **Report date:** 2023-10-04

- **Voluntary/Mandated:** N/A
- **Location:** Saint Petersburg, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2636-2023

## Citation

> AI Analytics. FDA recall Z-2636-2023. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2636-2023. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
