{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tustin",
      "address_1": "PO Box 2068",
      "reason_for_recall": "During a procedure the Peak Skin Dose (PSD) value was displayed on the DTS larger than the DTS expected value. It was found that the software incorrectly calculated the PSD value when the x-ray condition of the frontal plane and the lateral plane are the same. It incorrectly used in the calculation a dose value from a previous exposure.",
      "address_2": "2441 Michelle Dr",
      "product_quantity": "23",
      "code_info": "Model Number - XIDF-AWS801",
      "center_classification_date": "20160718",
      "distribution_pattern": "US Distribution to the states of : NC, NY, TX, GA, CA, AZ, IL, FL,MA, MO and DE.",
      "state": "CA",
      "product_description": "Toshiba America Medical Systems Angio WorkStation: XIDF-AWS801v6.00, v6.01, and V6.10 System: INFX-8000V Bi-Plane System",
      "report_date": "20160727",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-2188-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74473",
      "termination_date": "20170425",
      "more_code_info": "",
      "recall_initiation_date": "20160224",
      "postal_code": "92780-7047",
      "voluntary_mandated": "FDA Mandated",
      "status": "Terminated"
    }
  ]
}