{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Hartland",
      "address_1": "900 Walnut Ridge Dr",
      "reason_for_recall": "This recall has been initiated due to an issue related to the potential accidental deletion of record(s) by an Eye Station user.",
      "address_2": "",
      "product_quantity": "1597 (1451 US;  146 OUS)",
      "code_info": "Merge Eye Station software versions: 11.6.0 and prior",
      "center_classification_date": "20170112",
      "distribution_pattern": "US:   Alabama, Alaska, Arizona,Arkansas, California,Colorado,Connecticut,Delaware,  District of Columbia, Georgia,Hawaii, Idaho, Illinois,Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland,Massachusetts, Michigan, Minnesota,   Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Florida, Tennessee, Wyoming.    OUS:  Czech Republic  Algeria  Belgium  Brazil  Canada  Denmark  France  Germany  Greece  India  Israel  Italy  Korea, Republic of  Luxembourg  Netherlands  Poland  Russian Federation  Singapore  United Kingdom",
      "state": "WI",
      "product_description": "Merge Eye Station  f/k/a: DFC-1024 & DFC-512 Digital Imaging System,  WinStation, and WinStation Retinal Imager distributed by Ophthalmic Imaging Systems (OIS).  Versions: 11.6.0 and prior",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-1017-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75602",
      "termination_date": "20210324",
      "more_code_info": "",
      "recall_initiation_date": "20161209",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}