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Open, Classified

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

FDA Recall Z-1807-2026 · Posted 2026-04-17

Recalling FirmUvlizer c/o RAIS INTERNATIONAL LLC
Recall StatusOpen, Classified
Product CodeRHP
Date Initiated2026-03-06
Product Quantity480,000

Reason for Recall

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.

Firm Action

Notifications to purchasers and subsequent transferees will be transmitted through multiple communication channels: Certified Mail, Email Notifications, and Public Website Notice, describing the defect, safety considerations, and instructions to discontinue use of the Product.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

U.S.

Official Source

View FDA Recall →

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

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