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Open, Classified

Mito Red Light, Super Mobile

FDA Recall Z-2478-2026 · Posted 2026-06-17

Recalling FirmMITO RED LIGHT INC
Recall StatusOpen, Classified
Product CodeILY
Date Initiated2025-02-12

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.

Firm Action

Beginning on on February 12, 2025, Mito Red Light LLC issued a recall notification to affected consignees in a variety of methods. Mito Red Light is asking consignees to take the following actions: 1. Immediately stop using the mito Mobile Super. 2. Do not charge the device. Disconnect any chargers from the device and rom any power outlet. 3. Store the device away from flammable materials, in a cool dry place, until you can dispose of it. 4. Contact Mito Mobile at 1-866-861-6486 , Email: [email protected], website: mitoredlight.com/pages/recall to request a replacement device.

Root Cause

Under Investigation by firm

Distribution Pattern

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.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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