FDA Medical Device Recalls (openFDA)
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 number
- Z-0457-2023
- Recalling firm
- PHONESOAP
- 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.
- Status
- Open, Classified
- Initiated
- 2022-08-30
- Posted
- 2022-12-16
- Terminated
- not on file
- Reason
- Excessive ultraviolet-C radiation
- Root cause
- Radiation Control for Health and Safety Act
- Action
- 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.
- Quantity
- 6,700 systems
- Distribution
- US Nationwide Distribution
- Lot, serial or model codes
- SurfaceSoap UV Disinfecting Wand
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- RHP
- Firm FEI
- 3016746333
- Firm city
- Provo
- Firm state
- UT
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28