{
  "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": "82612",
      "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": "Letter",
      "distribution_pattern": "Distribution was made to FL, IL, MI, MO,  NY, and WI.   There was no government/military distribution.  Foreign distribution was made to Denmark, France, Germany, Netherlands, South Korea, Switzerland, Turkey, UAE,",
      "recall_number": "Z-1251-2019",
      "product_description": "MRIdian Linac Radiation Therapy System, Model 20000.",
      "product_quantity": "17 devices",
      "reason_for_recall": "A discrepancy between optimization and planning forward dose calculation between adaptive optimizations and AQA dose calculations can occur.",
      "recall_initiation_date": "20190318",
      "center_classification_date": "20190502",
      "termination_date": "20220616",
      "report_date": "20190508",
      "code_info": "Serial Numbers 101,107, 201, 202, 203, 204, 205, 206, 209,  211, 213, 214, 217, 221, 223, 225, 228."
    }
  ]
}