FDAOctober 26, 2021device
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.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Excessive ultraviolet-C radiation
What to do
FDA enforcement status: Ongoing
Brands named
max luxmax
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- CPSCBabysense Max View Baby Monitors Recalled Due to Fire Hazard; Manufactured by Hisense2026-02-26
- FDAMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.2025-08-12
- FDAMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCMC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.2025-08-12
- FDAMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.2025-08-12
- CPSCKramer Laboratories Recalls Safetussin Max Strength Multi-Symptom Cough, Cold and Flu Blister Packs Due to Risk of Child Poisoning; Violation of Federal Regulation for Child Resistant Packaging2025-04-10
- FDAMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.2024-12-20
- FDAMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.2024-12-20
- CPSCBrandline Recalls HEAO High Chairs Due to Risk of Suffocation, Entrapment and Laceration Hazards; Violation of the Federal Safety Standards; Sold Exclusively on Amazon.com2023-12-21
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