The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission
FDA device recall Z-1807-2026 · posted 2026-04-17 · Open, Classified
Recall details
- Recalling firm
- Uvlizer c/o RAIS INTERNATIONAL LLC
- 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.
- Action taken
- 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
- Status
- Open, Classified
- Product code
- RHP
- Quantity affected
- 480,000
- Distribution
- U.S.
- Date initiated
- 2026-03-06
- Date posted
- 2026-04-17
- Location
- Lewes, DE
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