{
  "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": "Oakwood Village",
      "address_1": "2 Thermo Fisher Way",
      "reason_for_recall": "The system loaded a completion fraction in the incorrect order after a treatment interruption.",
      "address_2": "",
      "product_quantity": "5 units",
      "code_info": "Model #: 10000, Serial #'s: 100, 101, 102, 104 & 105",
      "center_classification_date": "20160212",
      "distribution_pattern": "US Distribution to the states of : CA, FL, MO & WI., and Internationally to Republic of Korea.",
      "state": "OH",
      "product_description": "MRIdian ViewRay Radiation Therapy System, VIEWRAY Inc.",
      "report_date": "20160224",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Viewray Incorporated",
      "recall_number": "Z-0806-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73086",
      "termination_date": "20170222",
      "more_code_info": "",
      "recall_initiation_date": "20151224",
      "postal_code": "44146-6536",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}