FDA Medical Device Recalls (openFDA)
MAX LUX CORP: The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.
- Recall number
- Z-0246-2022
- Recalling firm
- MAX LUX CORP
- Product
- The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.
- Status
- Open, Classified
- Initiated
- 2021-10-26
- Posted
- not on file
- Terminated
- not on file
- Reason
- Excessive ultraviolet-C radiation
- Root cause
- Radiation Control for Health and Safety Act
- Action
- not on file
- Quantity
- 9900 units
- Distribution
- US Nationwide Distribution
- Lot, serial or model codes
- Safe-T Lite
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- RHP
- Firm FEI
- 3017032819
- Firm city
- not on file
- Firm state
- not on file
- 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