{
  "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": "75425",
      "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 AZ, CA, ID, IL, IN, MI, MN, and NJ.",
      "recall_number": "Z-0294-2017",
      "product_description": "Fusion Workstation.; Indicated for the transmission and review of radiological images.",
      "product_quantity": "13 sites potentially hae the affected version",
      "reason_for_recall": "After a period of time running Fusion Workstation, the Hounsfield measurement tool will report incorrect values.",
      "recall_initiation_date": "20111028",
      "center_classification_date": "20161020",
      "termination_date": "20161214",
      "report_date": "20161026",
      "code_info": "Versions V3.0.2 P3, 3.02, 3.1, 3.2, 3.3, and 3.3.1."
    }
  ]
}