{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Kashiwa",
      "state": "N/A",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98330",
      "recalling_firm": "Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha",
      "address_1": "44-141-1,W 226",
      "address_2": "Wakashiba",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US distribution to states of: TX, Washington DC",
      "recall_number": "Z-1429-2026",
      "product_description": "Brand Name: Hitachi Proton Beam Therapy System   Ref: PROBEAT-FR",
      "product_quantity": "1",
      "reason_for_recall": "Software anomaly in the patient positioning system may result in positional discrepancy.",
      "recall_initiation_date": "20260206",
      "center_classification_date": "20260220",
      "report_date": "20260304",
      "code_info": "Serial number: PTFR-01/ UDI:(01)04560333350204(11)240112(21)PTFR-01"
    }
  ]
}