{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "37400",
      "product_res_number": "Z-0494-05",
      "event_date_initiated": "2004-09-07",
      "event_date_created": "2015-06-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-02-10",
      "res_event_number": "31217",
      "product_code": "rad",
      "product_description": "X-Ray High Voltage Generator, Model KXO-80G used on Image Intensified Fluoroscopoc X-Ray System DUA-450D",
      "code_info": "All Serial numbers in domestic distribution.",
      "firm_fei_number": "2020563",
      "recalling_firm": "Toshiba American Med Sys Inc",
      "address_1": "2441 Michelle Dr",
      "city": "Tustin",
      "state": "CA",
      "postal_code": "92781",
      "additional_info_contact": "Paul Biggins\n714-730-5000",
      "reason_for_recall": "Non-compliance with Radiation Standards. Incorrect display of the radiographic time, due to software anomaly.",
      "root_cause_description": "Other",
      "action": "Firm sent recall letters to customers and will be following up with field corrections which will be made on-site by the firm's own employees.",
      "product_quantity": "494",
      "distribution_pattern": "Nationwide.",
      "openfda": {}
    }
  ]
}