{
  "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": "Hartland",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75497",
      "recalling_firm": "Merge Healthcare, Inc.",
      "address_1": "900 Walnut Ridge Dr",
      "address_2": "N/A",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distribution was made to medical facilities nationwide.  Foreign distribution was also made.",
      "recall_number": "Z-0611-2017",
      "product_description": "iConnect Access software.  The firm name on the label is Merge Healthcare, Hartland, WI.",
      "product_quantity": "60 sites potentially have the affected versions",
      "reason_for_recall": "Software displayed incorrect prior reports in the viewport area, only when more than one prior study (2 or more) was viewed.",
      "recall_initiation_date": "20160525",
      "center_classification_date": "20161117",
      "termination_date": "20190828",
      "report_date": "20161123",
      "code_info": "Versions 3.0.1, 3.1, and 3.2"
    }
  ]
}