{
  "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": "Oakwood Village",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72166",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Distribution to the states of :  CA, MO and WI., and Internationally to Korea.",
      "recall_number": "Z-0115-2016",
      "product_description": "MRIdian¿ ViewRay¿ Radiation Therapy System, ViewRay¿     Is indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.",
      "product_quantity": "4 units",
      "reason_for_recall": "ViewRay discovered that in the event that an encoder breaks or fails on the Patient Handling System (PHS, or couch), when attempting to restart the system, the couch could move unexpectedly.",
      "recall_initiation_date": "20150827",
      "center_classification_date": "20151009",
      "termination_date": "20170609",
      "report_date": "20151021",
      "code_info": "Catalog/Part Number: 10000; Serial Numbers: 100, 101, 102, & 105"
    }
  ]
}