{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Louvain La Neuve",
      "state": "",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80298",
      "recalling_firm": "Ion Beam Applications S.A.",
      "address_1": "Chemin du Cyclotron, 3",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of FL and the countries of Sweden, The Netherlands",
      "recall_number": "Z-2424-2018",
      "product_description": "Proteus 235, Version PTS-11.0.1.2 and PTS-11.0.2    Product Usage:  A device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.",
      "product_quantity": "3 units",
      "reason_for_recall": "Correction vector confirmation  message is lost if access point is changed after sending the correction vector.  As a result, the patient will be treated in the setup position or treatment position instead of the corrected position.",
      "recall_initiation_date": "20180516",
      "center_classification_date": "20180711",
      "termination_date": "20181016",
      "report_date": "20180718",
      "code_info": "Serial Numbers:  SAT.122 (EU)  SAT.132 (EU)  SAT.133 (US)",
      "more_code_info": ""
    }
  ]
}