{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tustin",
      "address_1": "2441 Michelle Dr",
      "reason_for_recall": "Although the Flat Panel Detector (FPD) touch sensor is activated during use, the error message is displayed and the audible signal continues sounding during the table movement of longitudinal tilt, the movement of longitudinal tilt does not stop.",
      "address_2": "P.O. Box 2068",
      "product_quantity": "2",
      "code_info": "Serial Numbers: ULD1412014, UUC13Z2011, A4A113Z2001.",
      "center_classification_date": "20140604",
      "distribution_pattern": "Nationwide Distribution including CA and IN",
      "state": "CA",
      "product_description": "Toshiba Infinix X-Ray Interventional System  INFX-8000V/UU.  An X-Ray system that is capable of radiographic and fluoroscopic studies used in an interventional setting.",
      "report_date": "20140611",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-1714-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68363",
      "termination_date": "20141002",
      "more_code_info": "",
      "recall_initiation_date": "20140512",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}