{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Aizuwakamatsu",
      "state": "",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90664",
      "recalling_firm": "Aizu Olympus Co., Ltd.",
      "address_1": "1 Chome 1-1",
      "address_2": "Niiderakita",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of FL, IL, NC, PA & TX.",
      "recall_number": "Z-1559-2022",
      "product_description": "EVIS EXERA III Bronchovideoscope",
      "product_quantity": "",
      "reason_for_recall": "The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.",
      "recall_initiation_date": "20220720",
      "center_classification_date": "20220819",
      "termination_date": "20250122",
      "report_date": "20220831",
      "code_info": "UDI-DI: 04953170342134; Serial No. 2911858; Model No. BF-XP190.",
      "more_code_info": ""
    }
  ]
}