{
  "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": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97441",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "",
      "postal_code": "18034-8229",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "US Nationwide Distribution.",
      "recall_number": "Z-0056-2026",
      "product_description": "EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180",
      "product_quantity": "1,070 units US; 2,180 units OUS",
      "reason_for_recall": "Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.",
      "recall_initiation_date": "20250911",
      "center_classification_date": "20251016",
      "report_date": "20251022",
      "code_info": "Model No. BF-P180; UDI: 4953170339288; All Serial No.",
      "more_code_info": ""
    }
  ]
}