{
  "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": "It was found that during a procedure the Peak Skin Dose (PSD) value displayed by the Dose Tracking System (DTS) was larger than the DTS expected value. This issue occurs when the power for the Angio Workstation is turned on after the power for the Infinix system is turned on.",
      "address_2": "2441 Michelle Dr",
      "product_quantity": "US - 70 systems",
      "code_info": "S/N : 8181622393",
      "center_classification_date": "20170530",
      "distribution_pattern": "US Distribution to the states of :LA, IL, NY, FL, MA, TN, MO, GA, CA, DE, MO, AL, ID, MN, TX, CT, PA, MS, OH, NC, NV, W VA,  WA,  AR,  NJ, MD, OK, IN and NH.",
      "state": "CA",
      "product_description": "Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F",
      "report_date": "20170607",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-2109-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77195",
      "termination_date": "20180606",
      "more_code_info": "",
      "recall_initiation_date": "20170201",
      "postal_code": "92780-7047",
      "voluntary_mandated": "FDA Mandated",
      "status": "Terminated"
    }
  ]
}