{
  "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": [
    {
      "status": "Terminated",
      "city": "Hartland",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75876",
      "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": "Other",
      "distribution_pattern": "Distribution was made to medical facilities located in MT, CA, PA, and TX.",
      "recall_number": "Z-0939-2017",
      "product_description": "DR Systems Unity PACS software, now known as Merge Unity PACS software.",
      "product_quantity": "9 sites potentially have the effected software",
      "reason_for_recall": "The software fails to associate to the correct MG image if there are two images for the same view.",
      "recall_initiation_date": "20151015",
      "center_classification_date": "20161230",
      "termination_date": "20210423",
      "report_date": "20170111",
      "code_info": "Version 11.0"
    }
  ]
}