Uvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure merc
- Recalling company
- Uvlizer c/o RAIS INTERNATIONAL LLC
- 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.
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 6, 2026
- Reported
- Apr 29, 2026
- Distribution
- U.S.
- Status
- Ongoing
- Quantity
- 480,000
- Lot / codes
- None provided.
- Company location
- Lewes, DE
- Recall type
- FDA Mandated
- Recall number
- Z-1807-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1807-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.