# FDA recall Z-1807-2026

> **Uvlizer c/o RAIS INTERNATIONAL LLC** · Class II · device recall initiated 2026-03-06.

## Product

The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm.

## 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.

## Key facts

- **Recall number:** Z-1807-2026
- **Recalling firm:** Uvlizer c/o RAIS INTERNATIONAL LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-06
- **Report date:** 2026-04-29

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Lewes, DE, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1807-2026

## Citation

> AI Analytics. FDA recall Z-1807-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1807-2026. Source: US FDA. Licensed CC0.

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