{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Louvain La Neuve",
      "state": "",
      "country": "Belgium",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79230",
      "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": "Nationally",
      "recall_number": "Z-0938-2018",
      "product_description": "Proteus 235, Proton Therapy System a medical device designed to produce and delivers a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.",
      "product_quantity": "37",
      "reason_for_recall": "There is a risk of misalignment of the patient when using treatment  plans with multiple isocenters.",
      "recall_initiation_date": "20171117",
      "center_classification_date": "20180309",
      "termination_date": "20210614",
      "report_date": "20180321",
      "code_info": "PAT.000 (US), PAT.001 (CN), PAT.003 (KR), PAT.006 (US), PAT.107  (EU), PAT.108 (US), PAT.109 (US), PAT.110 (US), PAT.111 (EU),  PAT.112 (US), PAT.113 (US), PAT.114 (EU), PAT.115 (EU), SAT.116  (US), SAT.117 (EU), SAT.119 (US), SAT.120 (EU), SAT.122 (EU),  SAT.123 (US), SAT.126 (US), SAT.132 (EU), SAT.133 (US), SBF.101  (EU), SBF.105 (US)",
      "more_code_info": ""
    }
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}