Uvlizer Handheld UV-C Germicidal Wand Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
The FDA has mandated a recall of approximately 480,000 Uvlizer handheld UV-C germicidal wands due to potential overexposure to UVC radiation exceeding safety guidelines.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 8, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
The FDA has mandated a recall of the Uvlizer handheld ultraviolet-C germicidal wand because, in some foreseeable use conditions, it can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
Which Products Are Affected
The affected product is a handheld ultraviolet-C germicidal wand that contains two low-pressure mercury bulbs with a peak emission wavelength at 254 nm, manufactured by Uvlizer c/o RAIS INTERNATIONAL LLC. Approximately 480,000 units are involved, distributed in the U.S. No specific model numbers, UPCs, or code information were provided.
What You Should Do
Consumers should immediately stop using the product and contact the recalling firm at RAIS INTERNATIONAL LLC, located at 16192 Coastal Hwy, Lewes, DE 19958-3608, for information on returns and refunds.
Why This Matters
This recall involves a large quantity of devices and underscores the potential risks of UVC radiation exposure, which could affect user safety in everyday use.
Source
Information from the FDA, recall number Z-1807-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,143 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to May 8, 2026.
Frequently Asked Questions
Common questions about this FDA recall.