MITO RED LIGHT INC recalls Mito Red Light
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.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Mito Red Light, Super Mobile
Lot / code information
All Serial/Lot numbers/No UDI
What the firm is doing
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: recall@mitoredlight.com, website: mitoredlight.com/pages/recall to request a replacement device.
DistributionShow detailsHide
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.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-2478-2026
- FDA device classification · ILYOfficial FDA classification for this device type
- CFR regulation · 21 CFR 890.5500The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find MITO RED LIGHT INCSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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