The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights. The
Summary
The FDA issued a Class II for The product is a handheld ultraviolet-C germicidal wand and contains a combinati by Uvlizer c/o RAIS INTERNATIONAL LLC. Reason: In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by inter.
Details
Source
Device Recall
External ID
Z-1808-2026
Action Date
2026-04-29
Status
Ongoing
Category
device
Product 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.
Lot/Code Info: None provided.
Quantity Affected: 334
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.
Distribution
U.S.
Type: FDA Mandated
Recall Initiated: 2026-03-06
Company
Lewes, DE
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 217 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Uvlizer c/o RAIS INTERNATIONAL LLC has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Uvlizer c/o RAIS INTERNATIONAL LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Uvlizer c/o RAIS INTERNATIONAL LLC have FDA actions?
Uvlizer c/o RAIS INTERNATIONAL LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1808-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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