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Recall Observatory FDA recall evidence

Device product

The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.

Z-1807-2026

March 06, 2026

Class II

Product summary

Firm
Uvlizer c/o RAIS INTERNATIONAL LLC
Event
Event 98747
Status
Ongoing
Classification
Class II
Quantity
480,000
Official record key
device-enforcement:Z-1807-2026

Official wording

Reason: In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.

Code information: None provided.

Distribution pattern: U.S.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.