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Open, Classified

ProSun International Luxura Vegaz, Model 52X; Ultraviolet Tanning Device

FDA Recall Z-2636-2023 · Posted 2023-09-28

Recalling FirmJ&T Health and Wellness LLC
Recall StatusOpen, Classified
Product CodeLEJ
Date Initiated2023-03-31
Product Quantity12 units

Reason for Recall

In some cases the communication isolator installed in the Model 52X can cause a disturbance in the glass-filter safety circuit.

Firm Action

ProSun INTERNATIONAL notified their consignees by email on 04/19/2023 a potential safety issue with their tanning beds. The notice explained the issue and requested the consignee cease use until the correction of the device can be conducted.

Root Cause

Other

Distribution Pattern

US

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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