{
  "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": "Alpharetta",
      "address_1": "5995 Winward Plaza",
      "reason_for_recall": "McKesson Cardiology Hemo front-end parameter boxes must undergo annual  maintenance testing to establish the proper functioning of the parameter boxes,  and to identify in a timely manner whether a parameter box is out of calibration.    McKesson has identified that its communication to customers regarding the  required maintenance tests was insufficient. While each unit has an attached  sticker i",
      "address_2": "Information Technology Business",
      "product_quantity": "625 devices",
      "code_info": "McKesson Cardiology TM Hemo versions: 11.0HF5, 11.1, 11.1SP5, 11.1SP6, 11.1SP6HF1, 11.1SP6HF3, 12SP1, 12.1, 12.1HF1, 12.1HF2, 12.2, 12.2HF1, 12.2HF2, 12.2HF3, 12.2HF4.",
      "center_classification_date": "20141020",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of Australia, Botswana, Canada, Germany, New Zealand, Netherlands, Pakistan, Portugal, South Africa, Turkey and The United Kingdom.",
      "state": "GA",
      "product_description": "McKesson Cardiology Hemo.    McKesson Cardiology\" Hemo is intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.",
      "report_date": "20141029",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Mckesson Information Solutions LLC",
      "recall_number": "Z-0093-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69380",
      "termination_date": "20171026",
      "more_code_info": "",
      "recall_initiation_date": "20140625",
      "postal_code": "30005",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}