{
  "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": [
    {
      "status": "Terminated",
      "city": "Tustin",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79153",
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "address_1": "PO Box 2068",
      "address_2": "2441 Michelle Dr",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "United States",
      "recall_number": "Z-0842-2018",
      "product_description": "INFX-8000F Fluoroscopic X-Ray Systems",
      "product_quantity": "17 units",
      "reason_for_recall": "During an examination a device error occurred and the ceiling drive operation was disabled. It was found that the fastening bolts of the driving portion of the ceiling drive loosened cause the error.",
      "recall_initiation_date": "20171229",
      "center_classification_date": "20180302",
      "termination_date": "20231129",
      "report_date": "20180314",
      "code_info": "Serial Numbers:   AHA1592004,  AGB1482001,  AHA1482001,  AGA1492002,  AHA14Z2002,  AGA1552003,  UUB13Y2039,  AHA15Y2005,  AHA1612006,  AHB1662007,  AGB1682004,  AGB1692005,  AGB16Z2006,  AHB1712008,  AHB1712009,  AGB1712007,  AHA1582003"
    }
  ]
}