{
  "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": "HIROSHIMA",
      "state": "N/A",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70638",
      "recalling_firm": "MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK",
      "address_1": "6-22, 4-CHOME, KAN-ON-SHIN-MACHI",
      "address_2": "NISHI-KU",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - US including FL, NY, OH, & TX, **Internationally - Belgium, Italy, Korea, France & Germany.",
      "recall_number": "Z-1574-2015",
      "product_description": "MHI-TM2000 Linear Accelerator System (Software Version 3.5.0 and 3.5.1)",
      "product_quantity": "11 units total",
      "reason_for_recall": "The operator console allows users to deliver therapeutic radiation to patients even though a specific communication error relevant to imaging conditions has occurred. In addition, the treatment record (the delivered radiation record) cannot be saved.",
      "recall_initiation_date": "20150417",
      "center_classification_date": "20150501",
      "termination_date": "20170411",
      "report_date": "20150513",
      "code_info": "Serial Numbers: 201902, 201903, 202903, 202905, 203901, 203902, 203903, 203905, 203906, 203919 & 203924"
    }
  ]
}