The Recall Desk
HighFDA (Devices)·Z-2478-2026·Announced 2026-06-24

Mito Red Light Super Mobile batteries may catch fire

The Mito Red Light Super Mobile near-infrared therapy device is being recalled because its lithium-ion battery may malfunction, causing it to catch fire or burst into flames.

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: FDA Class II recall with a stated fire hazard from a lithium-ion battery, a risk of harm with no injuries reported in the source.

Plain-English summary

The Mito Red Light Super Mobile, from Mito Red Light Inc, is being recalled. The recall applies to all serial and lot numbers; the notice states there is no UDI.

The stated reason is that the near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames. The FDA classified the action as Class II.

Distribution was worldwide, including nationwide in the United States across a large number of states.

Users should identify affected devices by the product name above and follow the instructions issued by Mito Red Light.

The recalled product

Product
Mito Red Light, Super Mobile
Manufacturer
MITO RED LIGHT INC
Category
Medical Device — Light therapy device
Hazard

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.

The notice also names 46 states specifically:

Related recalls

Same hazard · lithium ion battery

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