{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Kashiwa",
      "state": "N/A",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79439",
      "recalling_firm": "Hitachi Ltd., Medical System Operations Group",
      "address_1": "2-1",
      "address_2": "Shintoyofuta",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution in the state of NY.",
      "recall_number": "Z-1585-2018",
      "product_description": "MHI-TM2000 Linear Accelerator System    Product Usage:  MHI-TM2000 Linear Accelerator System is intended for radiation therapy of lesions, tumors and conditions anywhere in the body where radiation treatment is indicated.",
      "product_quantity": "1",
      "reason_for_recall": "Due to a system controller software anomaly, the patient positioning deviation correction may not be applied and may result in the wrong part of the patient being irradiated.",
      "recall_initiation_date": "20171208",
      "center_classification_date": "20180501",
      "termination_date": "20190411",
      "report_date": "20180509",
      "code_info": "Serial Number: 203919"
    }
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}