FDA Medical Device Recalls (openFDA)
MITO RED LIGHT INC: Mito Red Light, Super Mobile
- Recall number
- Z-2478-2026
- Recalling firm
- MITO RED LIGHT INC
- Product
- Mito Red Light, Super Mobile
- Status
- Open, Classified
- Initiated
- 2025-02-12
- Posted
- 2026-06-17
- Terminated
- not on file
- Reason
- The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
- Root cause
- Under Investigation by 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: recall@mitoredlight.com, website: mitoredlight.com/pages/recall to request a replacement device.
- Quantity
- not on file
- 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, 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.
- Lot, serial or model codes
- All Serial/Lot numbers/No UDI
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- ILY
- Firm FEI
- 3015313684
- Firm city
- Scottsdale
- Firm state
- AZ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28