{
  "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": "A situation can occur allowing two physicians to access the same study report in EchoIMS when launched from the Cardio Study List without receiving the read-only notification prompt.",
      "address_2": "",
      "product_quantity": "17 sites potentially have the affected versions",
      "code_info": "Version 9.0.9 and earlier using EchoIMS.",
      "center_classification_date": "20170320",
      "distribution_pattern": "US Distribution was made to medical facilities in CA, FL, IL, MD, MO, OH, OK, TX, VT, and WI.  Military distribution was also made.",
      "state": "WI",
      "product_description": "Merge Cardio software using EchoIMS.  The firm name on the label is Merge Healthcare, Hartland, WI.",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-1415-2017",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "76401",
      "termination_date": "20170320",
      "more_code_info": "",
      "recall_initiation_date": "20160404",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}