{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Scottsdale",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98999",
      "recalling_firm": "MITO RED LIGHT INC",
      "address_1": "9319 N 94th Way Ste 400",
      "address_2": "",
      "postal_code": "85258-5565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide - 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.",
      "recall_number": "Z-2478-2026",
      "product_description": "Mito Red Light, Super Mobile",
      "product_quantity": "",
      "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.",
      "recall_initiation_date": "20250212",
      "center_classification_date": "20260617",
      "report_date": "20260624",
      "code_info": "All Serial/Lot numbers/No UDI",
      "more_code_info": ""
    }
  ]
}