{
  "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": "Mountain View",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84303",
      "recalling_firm": "Viewray, Inc.",
      "address_1": "815 E Middlefield Rd",
      "address_2": "N/A",
      "postal_code": "94043-4025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US - CA, FL, IL, MI, MO, NY, and WI    OUS: Denmark, France, Germany, Italy, Japan, Netherlands, Turkey, South Korea, and UAE",
      "recall_number": "Z-0676-2020",
      "product_description": "MRIdian Linac Radiation Therapy System Model 10000 and 20000",
      "product_quantity": "24 Systems",
      "reason_for_recall": "Issue with transferring treatment regiment from one system to another.  Adequate instructions for transferring treatment plan(s) are not provided within the operator's manual or within the software operating system.",
      "recall_initiation_date": "20190303",
      "center_classification_date": "20191212",
      "termination_date": "20210428",
      "report_date": "20191218",
      "code_info": "Serial Numbers: 100, 101, 102, 103, 104, 105, 107, 108, 112, 113, 201, 202, 203, 204, 205, 206, 209, 211, 213, 214, 217, 221, 223, 225    Device Listing Number: D158423 and D297999",
      "more_code_info": ""
    }
  ]
}