Class II — MITO RED LIGHT INC
| Recalling firm | Mito Red Light |
|---|---|
| Registered facility | Mito Red Light LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames. |
| Product | Mito Red Light, Super Mobile |
| 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. |
| Initiated | 2025-02-12 |
| Classified | 2026-06-17 |
| Recall number | Z-2478-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — MITO RED LIGHT INC (Z-2478-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98999/
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