{
  "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": "76654",
      "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": "USA (nationwide ) Distribution to medical facilities. Government distribution was also made.  There was no foreign or military distribution.",
      "recall_number": "Z-1470-2017",
      "product_description": "iConnect Enterprise Archive when used with RadSuite.  The firm name on the label is Merge Healthcare.",
      "product_quantity": "187 sites potentially have the affected versions",
      "reason_for_recall": "The software produced a number of \u001c\"do not route\"\u001d exceptions, which may result in potential patient injury or delay in diagnosis or treatment.",
      "recall_initiation_date": "20160404",
      "center_classification_date": "20170315",
      "termination_date": "20190828",
      "report_date": "20170322",
      "code_info": "iConnect Enterprise Archive versions 5.30.0 thru 9.4.3 and V11.0."
    }
  ]
}