{
  "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": [
    {
      "country": "United States",
      "city": "Palo Alto",
      "address_1": "911 Hansen Way",
      "reason_for_recall": "Modifications in version 13.6MR2 for Contouring, SmartAdapt, and SmartSegmentation workspaces resulted in contours not being saved consistently in Eclipse. Treatment Planning System. The issue only occurs if certain conditions are fulfilled.",
      "address_2": "",
      "product_quantity": "42 devices are affected",
      "code_info": "Model # H48    Serial numbers:  H48L574  H48L575  H48L576  H48L577  H48L578  H48L579  H48L580  H48L581  H48L582  H48L583  H48L584  H48L585  H48L586  H48L587  H482484  H487302  H48A587  H48D957  H480113  H480118  H481884  H481885  H481886  H481916  H481917  H484198  H484199  H488949  H48A680  H48A871  H48A872  H48A873  H48A874  H48A875  H48A876  H48A877  H48A878  H48A879  H48I531  H481195  H481236  H481237.",
      "center_classification_date": "20170110",
      "distribution_pattern": "US Distribution to the states of : NJ, TN. OR and FL.",
      "state": "CA",
      "product_description": "Eclipse Treatment Planning System version 13.MR2 [13.06.31  with Smart Segmentation Knowledge Based Contouring version 2.3 [2.3.12]      Radiology: The Eclipse Treatment Planning System (Eclipse TPS) is used to plan radiotherapy treatments for patients  with malignant or benign diseases. Eclipse TPS is used to plan external beam irradiation with photon, electron  and proton beams, as well as for internal irradiation (brachytherapy) treatments.",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Varian Medical Systems, Inc.",
      "recall_number": "Z-0990-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76018",
      "termination_date": "20170512",
      "more_code_info": "",
      "recall_initiation_date": "20161202",
      "postal_code": "94304-1028",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}