- Recalling firm
- Uvlizer c/o RAIS INTERNATIONAL LLC
- 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.
- Affected products (lot / model / serial)
- None provided.
- Units affected
- 480,000
- Distribution pattern
- U.S.
- Firm location
- Lewes, DE, United States
- Recall type
- FDA Mandated
- How the firm notified customers
- N/A
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1807-2026
- Recall initiated
- March 6, 2026
- FDA classification date
- April 17, 2026
- FDA report date
- April 29, 2026
- FDA event ID
- 98747
- Last updated on HTM Vibe
- July 24, 2026