{
  "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": "Cardio study list does not show STAT studies without refreshing.",
      "address_2": "",
      "product_quantity": "217 sites potentially have the affected versions",
      "code_info": "Versions 9.0; 9.0.1; 9.0.2; 9.0.3; 9.0.4; 9.0.5; 9.0.6; 9.0.7, 9.0.8, 9.0.9, 10.0, 10.0.1, 10.1, 10.1.1, and 10.1.2.",
      "center_classification_date": "20170319",
      "distribution_pattern": "Distribution was nationwide to medical facilities.  There was also military distribution.  There was no foreign/government distribution.",
      "state": "WI",
      "product_description": "Merge Cardio software.",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-1486-2017",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "76431",
      "termination_date": "20190726",
      "more_code_info": "",
      "recall_initiation_date": "20160404",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}