{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Tel Aviv",
      "state": "N/A",
      "country": "Israel",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70144",
      "recalling_firm": "McKesson Israel Ltd.",
      "address_1": "4 Nehoshet St., or Towers",
      "address_2": "Bldg. B",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including MA, MS, NH, NC, TX, WA and Internationally to the United Kingdom.",
      "recall_number": "Z-0910-2015",
      "product_description": "McKesson Cardiology ECG Management    It is a software application designed to import, display, store, analyze, distribute and manage information related to ECG procedures of adult and pediatric patients from external ECG devices.",
      "product_quantity": "9",
      "reason_for_recall": "An ECG procedure time stamp is incorrect, due to a software error in the McKesson Cardiology ECG Management with software versions 13.1 and 13.1.1.",
      "recall_initiation_date": "20141219",
      "center_classification_date": "20150105",
      "termination_date": "20160225",
      "report_date": "20150114",
      "code_info": "MC13.1 and MC13.1.1",
      "more_code_info": ""
    }
  ]
}