FDA Mandated Recall of Uvlizer Handheld UV-C Germicidal Wand
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 334 Uvlizer handheld UV-C germicidal wands due to potential exposure to UVC radiation exceeding safety limits.
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 "medium" 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.
Recall Article
What Happened
The products 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 products are handheld ultraviolet-C germicidal wands from Uvlizer c/o RAIS INTERNATIONAL LLC. The product comes in two configurations: UV-C x 1 and UV-A x 4, or UV-C x 2 and UV-A x 3, with peak emission wavelengths at 274 nm and 397 nm. A total of 334 units were distributed in the U.S., with recall number Z-1808-2026.
What You Should Do
Consumers should stop using the product and contact the recalling firm, Uvlizer c/o RAIS INTERNATIONAL LLC, for instructions on returns or refunds.
Why This Matters
This recall highlights potential health risks from excessive UV radiation exposure in consumer devices, underscoring the need for adherence to safety standards.
Source
FDA Recall Notice: Attribution to FDA, event ID 98742
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 (984 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 8, 2026.
Frequently Asked Questions
Common questions about this FDA recall.