{"url_path":"/fda/device/recalls/Z-2478-2026","section_key":"summary","section_title":"DEVICE Recall: MITO RED LIGHT INC — Mito Red Light, Super Mobile","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2025-02-12","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2478-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"MITO RED LIGHT INC"},"word_count":137,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2478-2026\n\n**Recalling firm:** MITO RED LIGHT INC\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2025-02-12\n**Report date:** 2026-06-24\n\n## Product\nMito Red Light, Super Mobile\n\n## Reason\nThe near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.\n\n## Affected lots\nAll Serial/Lot numbers/No UDI\n\n## Distribution\nWorldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, \tDE, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NL, NM, \tNV, 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."}