{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lexington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83524",
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "address_1": "81 Hartwell Ave Ste 300",
      "address_2": "N/A",
      "postal_code": "02421-3160",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-2441-2019",
      "product_description": "Fujifilm FDR Go Plus mobile X-ray system",
      "product_quantity": "174 units",
      "reason_for_recall": "The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)",
      "recall_initiation_date": "20190719",
      "center_classification_date": "20190830",
      "termination_date": "20200828",
      "report_date": "20190911",
      "code_info": "All serial numbers"
    }
  ]
}