FDAFDA · Food and drugs·Recall number Z-2478-2026
Mito Red Light, Super Mobile
Published June 24, 2026 · Recall initiated: February 12, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- MITO RED LIGHT INC
- Distributor
- Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NL, NM, NV, NY, OH, OR, PA, PR, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV and the countries of Australia, Canada, China, Japan, New Zealand, Spain, Switzerland, United Arab Emirates, United Kingdom.
- Lot
- All Serial/Lot numbers/No UDI
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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