{
  "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": "75239",
      "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": "Worldwide Distribution -  USA (nationwide) Distribution.  Foreign/military/government distribution was also made.",
      "recall_number": "Z-0137-2017",
      "product_description": "CADstream software.  The firm name on the label is Merge Healthcare, Hartland, WI.",
      "product_quantity": "844 sites potentially have the affected versions",
      "reason_for_recall": "The software was not presenting the PURE filter user interface message on DICOM transfer studies. If a site starts using PURE filter, the user interface message will not display.  This may result in incorrect patient follow-up.",
      "recall_initiation_date": "20160130",
      "center_classification_date": "20161019",
      "termination_date": "20201005",
      "report_date": "20161026",
      "code_info": "Versions prior to 5.2.9"
    }
  ]
}