{
  "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": "2026-04-15",
    "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": "76696",
      "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": "Distributed in MA, FL, VA, and TN.   China, South Korea, France and Germany",
      "recall_number": "Z-1695-2017",
      "product_description": "Proteus 235",
      "product_quantity": "8 worldwide, 4 in U.S.",
      "reason_for_recall": "The Proton Therapy System can allow gantry rotation even if the snout is not properly locked.",
      "recall_initiation_date": "20170309",
      "center_classification_date": "20170329",
      "termination_date": "20190326",
      "report_date": "20170405",
      "code_info": "Serial numbers: PAT.000, PAT.001, PAT.003, PAT.006, PAT.108, PAT.111, SAT.119, SAT.120",
      "more_code_info": ""
    }
  ]
}