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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices

J&T Health and Wellness LLC: Luxura Vegaz Model 52X Tanning Devices Recalled for Safety Circuit Fault

Agency Publication Date: September 28, 2023
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Summary

J&T Health and Wellness LLC is recalling 12 units of the ProSun International Luxura Vegaz, Model 52X Ultraviolet Tanning Device. The recall was initiated because the communication isolator component can interfere with the device's glass-filter safety circuit. This defect could compromise the safety mechanisms that monitor the ultraviolet filters, potentially leading to improper operation of the device during tanning sessions.

Risk

A disturbance in the safety circuit may prevent the device from detecting if the glass filters are missing or damaged. This could result in users being exposed to harmful levels of ultraviolet radiation, increasing the risk of skin damage or eye injury.

What You Should Do

  1. Identify if you have a ProSun International Luxura Vegaz, Model 52X Ultraviolet Tanning Device.
  2. Check the identification plate on your device for the following serial numbers: 52X0012, 52X0013, 52X0014, 52X0024, 52X0029, 52X0030, 52X0031, 52X0032, 52X0033, 52X0034, 52X0036, or 52X0037.
  3. If your serial number is listed, contact the manufacturer, J&T Health and Wellness LLC, for instructions on how to resolve the safety circuit issue.
  4. Contact your healthcare provider if you have concerns about skin health or potential overexposure related to the use of this device.
  5. For additional questions, contact the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer correction regarding communication isolator interference.

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: ProSun International Luxura Vegaz, Model 52X; Ultraviolet Tanning Device
Model / REF:
Model 52X
Lot Numbers:
52X0012
52X0013
52X0014
52X0024
52X0029
52X0030
52X0031
52X0032
52X0033
52X0034
52X0036
52X0037

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92217
Status: Active
Manufacturer: J&T Health and Wellness LLC
Manufactured In: United States
Units Affected: 12 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.