{
  "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": [
    {
      "status": "Terminated",
      "city": "Hakusanshi",
      "state": "N/A",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71628",
      "recalling_firm": "Eizo  Corporation",
      "address_1": "153",
      "address_2": "Shimokashiwano",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including OH, FL, IL, TX, OH, NY, AZ, and NJ.",
      "recall_number": "Z-2089-2015",
      "product_description": "RadiForce RX850, 8MP Color LCD Monitor, Part Code No. 0FTD1958A2, UPC 690592037180.  This product is intended to be used in displaying and viewing digital images those of digital mammography for review and analysis by trained medical practitioners.",
      "product_quantity": "2 units",
      "reason_for_recall": "EIZO is recalling the RadiForce LCD Monitors could display abnormally while connecting to particular graphics boards with DisplayPort.",
      "recall_initiation_date": "20150707",
      "center_classification_date": "20150716",
      "termination_date": "20161130",
      "report_date": "20150722",
      "code_info": "220045044, 20050044",
      "more_code_info": ""
    }
  ]
}