{
  "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": "67678",
      "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 Distribution including the states of  OK, IL, NJ, and WA.",
      "recall_number": "Z-1492-2014",
      "product_description": "Proteus 235 Proton Therapy System Legacy Software version 7.2.7 and higher, models 110, 112, 113, and 116.    Proton therapy",
      "product_quantity": "4",
      "reason_for_recall": "Internal testing of the Proteus 235 Proton Therapy System revealed incorrect dose rate calculation in case of beam line option other than Zero (0).",
      "recall_initiation_date": "20131204",
      "center_classification_date": "20140424",
      "termination_date": "20140612",
      "report_date": "20140430",
      "code_info": "Proteus 235 Proton Therapy System Legacy Software version 7.2.7 and higher, models 110, 112, 113, and 116.",
      "more_code_info": ""
    }
  ]
}