{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Twinsburg",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84133",
      "recalling_firm": "Hitachi Medical Systems America Inc",
      "address_1": "1959 Summit Commerce Park",
      "address_2": "N/A",
      "postal_code": "44087-2371",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The devices were distributed to the following US states:  CA, FL, GA, IA, IN, MD, MT, NC, NY, OH, OK, SD, TN, TX, WY, and PR.    The products were distributed to the following foreign countries:  Brazil and Mexico.",
      "recall_number": "Z-0271-2020",
      "product_description": "Hitachi Scenaria Whole-body X-ray CT System",
      "product_quantity": "39",
      "reason_for_recall": "There is a possibility that the cables to the controller unit may not be affixed properly, creating the potential for a cable to detach during scanning and eject from the system.",
      "recall_initiation_date": "20191016",
      "center_classification_date": "20191101",
      "termination_date": "20200430",
      "report_date": "20191113",
      "code_info": "Scenaria units S5002-S5014, S5017-S5044"
    }
  ]
}