{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Nishishirakawa-Gun",
      "state": "",
      "country": "Japan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93583",
      "recalling_firm": "Shirakawa Olympus Co., Ltd.",
      "address_1": "Azaokamiyama 3-1",
      "address_2": "Oazaodakura; Nishigo-Mura",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0692-2024",
      "product_description": "Model No. CYF-V2R, VISERA Cysto-Nephro Videoscope",
      "product_quantity": "608 US; 1264 OUS",
      "reason_for_recall": "Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.",
      "recall_initiation_date": "20231204",
      "center_classification_date": "20240109",
      "report_date": "20240117",
      "code_info": "UDI-DI: 04953170339523 04953170411212    All serial numbers",
      "more_code_info": ""
    }
  ]
}