MITO RED LIGHT INC recalls Mito Red Light
- Recalling company
- MITO RED LIGHT INC
- Product
- Mito Red Light, Super Mobile
- Reason
- The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 12, 2025
- Reported
- Jun 24, 2026
- Distribution
- 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.
- Status
- Ongoing
- Lot / codes
- All Serial/Lot numbers/No UDI
- Company location
- Scottsdale, AZ
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2478-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2478-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.