Scottsdale, AZ, United States
MITO RED LIGHT INC recalls
1 recall recorded since 2018, most recently on 12 February 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 12 February 2025
- Reason
- The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
- 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
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2478-2026
- Mito Red Light, Super Mobile
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.