[pending] Mito Red Light, Super Mobile
Pending LLM rewrite. Source: FDA_DEVICE Z-2478-2026.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Pending LLM scoring against the rubric.
Plain-English summary
The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
The recalled product
- Product
- Mito Red Light, Super Mobile
- Manufacturer
- MITO RED LIGHT INC
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All Serial/Lot numbers/No UDI
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- ModerateKL Owen Custom Orthodontic Solution bracket placement defect
FDA (Devices) · 2026-07-15
- HighMiniMed 780G Insulin Pump Software Anomaly Recall
FDA (Devices) · 2026-07-15
- ModerateAquacel Ag Surgical SP Surgical Dressing Recalled for Out-of-Specification Thickness
FDA (Devices) · 2026-07-15
- ModerateGSP Neonatal GALT Kit in vitro diagnostic test equipment
FDA (Devices) · 2026-07-15
- ModerateOlympus Single Use Distal Cover MAJ-2315 Duodenovideoscope Replacement
FDA (Devices) · 2026-07-15