FDA DevicesClass II
Mito Red Light, Super Mobile
Published: June 24, 2026Recall ID: Z-2478-2026Category: devicesCountry: US
Reason for Recall / Hazard
The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
Product Description & Identification
Mito Red Light, Super Mobile
Additional Source Details
| Field | Value |
|---|---|
| City | Scottsdale |
| State | AZ |
| Event id | 98999 |
| Address 1 | 9319 N 94th Way Ste 400 |
| Code info | All Serial/Lot numbers/No UDI |
| Postal code | 85258-5565 |
| Report date | 20260624 |
| Product type | Devices |
| Reason for recall | The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20250212 |
| Initial firm notification | |
| Center classification date | 20260617 |
Overview
- Recalling FirmMITO RED LIGHT INC
- StatusOngoing
- Risk LevelClass II
- DistributionWorldwide - 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.