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Open, Classified

The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.

FDA Recall Z-0246-2022 · Posted None

Recalling FirmMAX LUX CORP
Recall StatusOpen, Classified
Product CodeRHP
Date Initiated2021-10-26
Product Quantity9900 units

Reason for Recall

Excessive ultraviolet-C radiation

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US Nationwide Distribution

Official Source

View FDA Recall →

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

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