{
  "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": "Oakwood Village",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71555",
      "recalling_firm": "Viewray Incorporated",
      "address_1": "2 Thermo Fisher Way",
      "address_2": "N/A",
      "postal_code": "44146-6536",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of CA, MO & WI",
      "recall_number": "Z-2085-2015",
      "product_description": "Patient Handling System (Motion Control Software),     Product Usage:  Indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.",
      "product_quantity": "3",
      "reason_for_recall": "ViewRay received a report that the couch moved unexpectedly into the bore after performing a RTCS reboot.",
      "recall_initiation_date": "20150401",
      "center_classification_date": "20150716",
      "termination_date": "20160204",
      "report_date": "20150722",
      "code_info": "Model #10000, Serial #'s: 100, 101, and 102",
      "more_code_info": ""
    }
  ]
}