FDA Medical devices recall ·
The product is a handheld ultraviolet-C germicidal wand and contains a… recall
- Recall number
- Z-1808-2026
- Date
- (initiated March 6, 2026)
- Company / brand
- Uvlizer c/o RAIS INTERNATIONAL LLC
16192 Coastal Hwy, Lewes, DE, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 334
- Initiated by
- FDA Mandated
Read the official FDA notice ↗
Product
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 peak emission wavelengths at 274 nm and 397 nm.
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
None provided.
Distribution
U.S.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1808-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.