{
  "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": [
    {
      "status": "Terminated",
      "city": "Louvain La Neuve",
      "state": "N/A",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76804",
      "recalling_firm": "Ion Beam Applications S.A.",
      "address_1": "Chemin du Cyclotron, 3",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution in US (to Louisiana), and France.",
      "recall_number": "Z-1830-2017",
      "product_description": "Proteus 235, Proton Therapy System",
      "product_quantity": "2 worldwide, 1 in U.S.",
      "reason_for_recall": "In specific circumstances, the user is able to restart an aborted irradiation without having to select the correct partial irradiation data.",
      "recall_initiation_date": "20170321",
      "center_classification_date": "20170417",
      "termination_date": "20180919",
      "report_date": "20170426",
      "code_info": "Serial Number: SAT.123 (US), and  SBF.101 (EU). Versions PTS-9.3.1.2 and PTS-9.4.0"
    }
  ]
}