{
  "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": [
    {
      "country": "United States",
      "city": "Hartland",
      "address_1": "900 Walnut Ridge Dr",
      "reason_for_recall": "Patient information in the header is only found on the first page of the report and not on the subsequent pages.",
      "address_2": "",
      "product_quantity": "42 sites potentially have the affected version",
      "code_info": "Version 10.1",
      "center_classification_date": "20160921",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "WI",
      "product_description": "Merge Cardio software.      Product Usage:  Merge Cardio is an integrated cardiovascular information system classified as a picture archiving and communications system.",
      "report_date": "20160928",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-2865-2016",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "75034",
      "termination_date": "20171215",
      "more_code_info": "",
      "recall_initiation_date": "20160130",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}