{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Louvain-la-neuve",
      "state": "N/A",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86076",
      "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": "US: VA  OUS: Belgium",
      "recall_number": "Z-2715-2020",
      "product_description": "Proteus 235  The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical 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": "2 Units",
      "reason_for_recall": "IBA became aware of an issue to resume aborted irradiations because the plan to complete the treatment cannot be loaded.",
      "recall_initiation_date": "20200717",
      "center_classification_date": "20200727",
      "termination_date": "20210830",
      "report_date": "20200805",
      "code_info": "Serial Number: Manufacture date  SAT.140 (US): manufactured May 2019  SBF.112 (EU): manufactured October 2019"
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}