{
  "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": "System locks up which may result in potential patient injury or delay in diagnosis or treatment.",
      "address_2": "",
      "product_quantity": "78 sites potentially have the affected accessory",
      "code_info": "Versions 1.1.2 and 1.1.3",
      "center_classification_date": "20170320",
      "distribution_pattern": "Distribution was made USA (nationwide) to medical facilities. Government distribution was made.  Foreign distribution was made to Canada.  There was no military distribution.",
      "state": "WI",
      "product_description": "Merge Eye Station Import Utility (ESIU).  The firm name on the labeling is Merge Healthcare.",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-1498-2017",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "76312",
      "termination_date": "20200615",
      "more_code_info": "",
      "recall_initiation_date": "20160404",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}