{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88562",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "PO Box 610",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution nationwide. Product also distributed globally.",
      "recall_number": "Z-2564-2021",
      "product_description": "BF-N20 OES Bronchofiberscope, Model No. BF-N20",
      "product_quantity": "377",
      "reason_for_recall": "The firm is issuing validated, new reprocessing instructions according to the FDA 2015 guidance, \"Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling.\"",
      "recall_initiation_date": "20210816",
      "center_classification_date": "20210924",
      "termination_date": "20240311",
      "report_date": "20211006",
      "code_info": "All serial numbers"
    }
  ]
}