FDA Recall Open, Classified

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.

Recall: Z-1808-2026 · Initiated March 6, 2026

Recall

Recall Number
Z-1808-2026
Event Number
98742
Firm
Uvlizer c/o RAIS INTERNATIONAL LLC
FEI Number
3031733296
Product Code
RHP
Status
Open, Classified
Root Cause
Radiation Control for Health and Safety Act
Initiated
March 6, 2026
Posted
April 17, 2026
Address
16192 Coastal Hwy, Lewes, DE, 19958-3608

Description

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.

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.

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.

Distribution

U.S.

Quantity

334