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.
Take action
Contact the company
📍Recalling firmUvlizer c/o RAIS INTERNATIONAL LLC16192 Coastal Hwy · Lewes, DE 19958-3608
“Uvlizer Germicidal Wand Recalls: UVC Radiation Exposure Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49776-uvlizer-germicidal-wand-recalls-uvc-radiation-exposure-risk. Based on FDA recall #Z-1807-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1807-2026%22&limit=1).
The FDA announced on March 6, 2026, that Uvlizer c/o RAIS INTERNATIONAL LLC is recalling handheld ultraviolet-C germicidal wands due to the risk of excessive UVC radiation exposure. The agency mandated the recall of approximately 480,000 units distributed in the U.S.
How to tell if you have it
Brand: Uvlizer
Company: Uvlizer c/o RAIS INTERNATIONAL LLC
Product: Handheld ultraviolet-C germicidal wand with two low-pressure mercury bulbs
Quantity: 480,000 units
The hazard
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.
Context
GovInfoNow's records show that Uvlizer c/o RAIS INTERNATIONAL LLC has one other recall on record since March 6, 2026, involving the same risk of excessive UVC exposure. Other recent recalls of similar products include Daavlin Photera 600 UV Lamp (March 5, 2026), Daavlin Photera 600 3-D UV Lamp (March 5, 2026), and Lutronic DermaV Laser System Recall (August 6, 2026).
How to tell if you have this one
Check for Uvlizer germicidal wands with two low-pressure mercury bulbs emitting UVC radiation. The product was sold as a handheld device for disinfection purposes.
Brand
Uvlizer
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the brand name Uvlizer and the product description of a handheld UV-C germicidal wand with two low-pressure mercury bulbs.
How this recall unfolded
Recall timeline
FDA published this recall 54 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1807-2026 (March 6, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1807-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.