Z-1808-2026Class II

The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED...

Name: Z-1808-2026 The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED...
Creator: Uvlizer c/o RAIS INTERNATIONAL LLC
Published: 2026-03-06
License: https://open.fda.gov/license/

Uvlizer c/o RAIS INTERNATIONAL LLC / initiated 2026-03-06 / Open, Classified

FDA source

Uvlizer c/o RAIS INTERNATIONAL LLC began a recall of 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... on 2026-03-06. FDA classified it as Class II and gives the reason as "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". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-1808-2026
Classification: Class II
Status: Open, Classified
Initiated: 2026-03-06
Posted: 2026-04-17
Recalling firm: Uvlizer c/o RAIS INTERNATIONAL LLC
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.
Product code: RHP Uv Lamp, Germicidal
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.
FDA root cause: Radiation Control for Health and Safety Act
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.
Quantity in commerce: 334
Distribution: U.S.
Product codes and lots: None provided.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1808-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1808-2026	Class II	Ongoing	FDA Mandated	2026-04-29	2026-04-17

Product code RHP

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)