HIGHFDA DEVICE

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...

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.

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
March 6, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
March 6, 2026
Hazard Level
HIGH
Brand
Uvlizer c/o RAIS INTERNATIONAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Uvlizer c/o RAIS INTERNATIONAL
Model numbers
None provided.

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    March 6, 2026

  2. Reported by FDA DEVICE

    April 29, 2026

  3. RecallRadar source check

    May 6, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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 You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Uvlizer c/o RAIS INTERNATIONAL LLC or your healthcare provider for instructions. Notification method: N/A

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Full 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.. Classification: Class II. Quantity: 334. Distribution: U.S.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
None provided.
Report Date
April 29, 2026
Recall Status
ACTIVE