{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "6740 Top Gun St",
      "reason_for_recall": "Phillips Healthcare initiated this action because the Main Control Board (MCB) may produce an inaccurate low patient temperature reading and low temperature alarm.",
      "address_2": "",
      "product_quantity": "50",
      "code_info": "Model Numbers: 861470 (120V), 861472 (240V).",
      "center_classification_date": "20140127",
      "distribution_pattern": "Worldwide Distribution - US (Nationwide) and Internationally to: Austria, France, Germany The Netherlands, Spain, Sweden, and Switzerland.",
      "state": "CA",
      "product_description": "InnerCool RTx Endovascular System, Model Numbers: 861470 (120V), 861472 (240V).    Product Usage:  The InnerCool RTx device is a thermal regulating system intended to induce, maintain and reverse mild hypothermia, to achieve and/or maintain normothermia, and for use in fever reduction.      K080908",
      "report_date": "20140205",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Healthcare",
      "recall_number": "Z-0845-2014",
      "initial_firm_notification": "Other",
      "product_type": "Devices",
      "event_id": "67319",
      "termination_date": "20140213",
      "more_code_info": "",
      "recall_initiation_date": "20140113",
      "postal_code": "92121-4114",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}