{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Aizuwakamatsu",
      "state": "N/A",
      "country": "Japan",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93222",
      "recalling_firm": "Aizu Olympus Co., Ltd.",
      "address_1": "3 Chome 1-1",
      "address_2": "Niiderakita",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution.",
      "recall_number": "Z-0330-2024",
      "product_description": "Choleodochoscope. Model Numbers: CHF-BP30, CHF-CB30L, CHF-P60.",
      "product_quantity": "3 units",
      "reason_for_recall": "Channel air drying process was not validated, and that a small percentage of scopes returned to customers after repair had a wet channel. Water remaining in the channel of the endoscopes has the potential for contamination that could lead to the risk of infection",
      "recall_initiation_date": "20230925",
      "center_classification_date": "20231117",
      "report_date": "20231129",
      "code_info": "Model Number (UDI-DI): CHF-BP30 (04953170068751), CHF-CB30L (04953170340154), CHF-P60 (Not recorded).",
      "more_code_info": ""
    }
  ]
}