Atlas FDA

Mito Red Light, Super Mobile

FDA device recall Z-2478-2026 · posted 2026-06-17 · Open, Classified

Recall details

Recalling firm
MITO RED LIGHT INC
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.
Action taken
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.
Root cause
Under Investigation by firm
Status
Open, Classified
Product code
ILY
Distribution
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
Date initiated
2025-02-12
Date posted
2026-06-17
Location
Scottsdale, AZ

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.