{
  "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": "2026-04-29",
    "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": "71050",
      "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": "Telephone",
      "distribution_pattern": "US distribution to MO.",
      "recall_number": "Z-1580-2015",
      "product_description": "ViewRay System, Radiation Therapy System",
      "product_quantity": "1",
      "reason_for_recall": "The software was not correctly using the RT (Radiation Therapy) to MR (Magnetic Resonance image) coordinate correction for non HFS (Head First Supine) patient orientations, resulting in slice mismatch error.",
      "recall_initiation_date": "20150115",
      "center_classification_date": "20150505",
      "termination_date": "20150923",
      "report_date": "20150513",
      "code_info": "M/N 10000, S/N 100 only"
    }
  ]
}