Lewes, DE, United States
Uvlizer c/o RAIS INTERNATIONAL LLC recalls
2 recalls recorded since 2018, most recently on 6 March 2026. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 6 March 2026
- 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.
- Distribution
- U.S.
- Initiated
- FDA Mandated
- Recall number
- Z-1808-2026
- The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The product comes in two configurations: UV-C x 1; UV-A x 4, or UV-C x 2; UV-A x 3. The product has two
Ongoing Class II Medical devices
- Recall started
- 6 March 2026
- 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.
- Distribution
- U.S.
- Initiated
- FDA Mandated
- Recall number
- Z-1807-2026
- The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.