{
  "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": "When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray came into the dose meter on the lateral side. As a result, the dose meter sent a minus value to the software. Consequently, the software defined the data as an \"abnormal value\" and it stopped displaying dose data and the dose data was lost. The following message was displayed, \"Dose meter abnormal, Dose info disabled\".",
      "address_2": "2441 Michelle Dr",
      "product_quantity": "4",
      "code_info": "Serial Numbers  ACA1492002, AAA1492001, W4B1442020, and W4B1432018.",
      "center_classification_date": "20160209",
      "distribution_pattern": "US Nationwide Distribution to OH and NY",
      "state": "CA",
      "product_description": "INFX-8000V Bi-Plane X-Ray Interventional System        X-ray systems",
      "report_date": "20160217",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-0752-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73078",
      "termination_date": "20160518",
      "more_code_info": "",
      "recall_initiation_date": "20150814",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}