{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Madison",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80933",
      "recalling_firm": "Accuray Incorporated",
      "address_1": "1240 Deming Way",
      "address_2": "N/A",
      "postal_code": "53717-1954",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution: United States (nationwide), and countries of: United Kingdom, Germany, France, Finland, Netherlands, Portugal, Hong Kong, Poland, Australia, United Arab Emirates, Thailand,  and Japan.",
      "recall_number": "Z-3211-2018",
      "product_description": "Ashland(TM) Box Film Ball Cube II EBT3, P/N: 027863-002 rev E     Product is used to calibrate CyberKnife systems",
      "product_quantity": "259 units",
      "reason_for_recall": "the Ball Cube II phantom calibration film was not manufactured within necessary dimensions and may introduce up to 0.5 mm of positional inaccuracy to the CyberKnife System",
      "recall_initiation_date": "20180831",
      "center_classification_date": "20180920",
      "termination_date": "20201216",
      "report_date": "20180926",
      "code_info": "All units with the Ashland Brand distributed between August 1, 2017 and July 31, 2018"
    }
  ]
}