Mito Red Light — Class II medical device recall Z-2478-2026
Ongoing recall by MITO RED LIGHT INC, reported 2026-06-24, distributed nationwide. The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire
| Recall number | Z-2478-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MITO RED LIGHT INC, Scottsdale, AZ, United States |
| Recall initiated | 2025-02-12 |
| Classified | 2026-06-17 |
| Reported by FDA | 2026-06-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, CH, CN, ES, GB, JP, NZ |
| Reason classes | device malfunction |
Product
Mito Red Light, Super Mobile
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2478-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.