{
  "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": "",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80217",
      "recalling_firm": "Ion Beam Applications S.A.",
      "address_1": "Chemin du Cyclotron, 3",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Units were distributed to Korea and Jacksonville, FL.",
      "recall_number": "Z-2284-2018",
      "product_description": "The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE)     Proteus 235, Beam Management System (PBS)",
      "product_quantity": "2",
      "reason_for_recall": "IBA is conducting a voluntary recall to address a PTS (Proton Therapy System) software issue and to reduce the risk related to this issue.",
      "recall_initiation_date": "20160411",
      "center_classification_date": "20180623",
      "termination_date": "20200325",
      "report_date": "20180704",
      "code_info": "PAT.003 and PAT.006",
      "more_code_info": ""
    }
  ]
}