PHONESOAP The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
Brand
PHONESOAP
Lot Codes / Batch Numbers
SurfaceSoap UV Disinfecting Wand
Products Sold
SurfaceSoap UV Disinfecting Wand
PHONESOAP is recalling The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps due to Excessive ultraviolet-C radiation. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Excessive ultraviolet-C radiation
Recommended Action
Per FDA guidance
PhoneSoap LLC (PhoneSoap) will send the notification letter by certified mail to all purchasers, dealers, distributors and any known subsequent transferees. As part of the Notification Letter, PhoneSoap will direct the purchasers, dealers, distributors and any known subsequent transferees to return the product to PhoneSoap using an enclosed, prepaid mailing label within 6 months of receipt of the letter. PhoneSoap will replace all returned SurfaceSoap UV devices with its closed-system PhoneSoap Go, free of charge.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026