{
  "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": "79227",
      "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": "WA",
      "recall_number": "Z-0930-2018",
      "product_description": "Proteus 235, graphite block 8",
      "product_quantity": "3",
      "reason_for_recall": "IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader",
      "recall_initiation_date": "20171017",
      "center_classification_date": "20180308",
      "termination_date": "20190329",
      "report_date": "20180314",
      "code_info": "PAT.115, SAT.116"
    }
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}