{
  "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": [
    {
      "country": "United States",
      "city": "Madison",
      "address_1": "1240 Deming Way",
      "reason_for_recall": "There is an unintended drop of a secondary collimator housing that can occur during housing Xchange(TM) workflows.  Specifically, during an automated housing Xchange, an interlock may interrupt this operation causing the collimator housing to partially attach.",
      "address_2": "",
      "product_quantity": "43 units",
      "code_info": "a) 032500-010:  CyberKnife VSI 9.6.x Robotic Radiosurgery System for Japan  Serial Numbers:  C0281, C0307    b) 033000-010:  CyberKnife VSI Robotic Radiosurgery System  Serial Numbers:  C0042, C0064, C0071, C0074, C0079, C0091, C0098, C0102, C0137, C0161, C0180, C0182, C0187, C0200, C0203, C0210, C0216, C0230, C0238, C0246, C0247, C0249, C0252, C0255, C0257, C0264, C0269,  C0270, C0273, C0274, C0276, C0277, C0284, C0293, C0294, C0304, C0305, C0322, C0323, C0325, C0326",
      "center_classification_date": "20190531",
      "distribution_pattern": "US & Italy, United Kingdom, Switzerland, Belgium, Canada, Germany, France, Japan, Poland, Netherlands, Luxembourg, Australia, Qatar, Latvia, Portugal, India, Hungary, Turkey, United Arab Emirates, Thailand",
      "state": "WI",
      "product_description": "CyberKnife VSI, Part Numbers:  a) 032500-010:  CyberKnife VSI 9.6.x Robotic Radiosurgery System for Japan  b) 033000-010:  CyberKnife VSI Robotic Radiosurgery System",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Accuray Incorporated",
      "recall_number": "Z-1697-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82664",
      "termination_date": "20210401",
      "more_code_info": "",
      "recall_initiation_date": "20180410",
      "postal_code": "53717-1954",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}