{
  "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": "The issue was identified as a firmware problem with the generator.",
      "address_2": "2441 Michelle Dr",
      "product_quantity": "18",
      "code_info": "Ser. No. U1A1692606",
      "center_classification_date": "20170830",
      "distribution_pattern": "US Distribution to the states of : LA, AR, IA, TX, IL, MN. MS, NJ, WV, SC, LA, WY, NC and CA.",
      "state": "CA",
      "product_description": "Toshiba America Medical Systems Ultimax Digital Fluoroscopic X-Ray System  Model: DREX-UI80    Ultimax is intended for gastrointestinal studies, vascular studies, general radiography, and fluoroscopy. The system has medical applications ranging from but not limited to: contrast-enhanced studies, support of endoscopic studies, nonvascular contrast-enhanced studies, nonvascular IVR, vascular contrast-enhanced studies support of vascular NR, and general radiography.",
      "report_date": "20170906",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-3070-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77679",
      "termination_date": "20200925",
      "recall_initiation_date": "20170315",
      "postal_code": "92780-7047",
      "voluntary_mandated": "FDA Mandated",
      "status": "Terminated"
    }
  ]
}