{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Center Valley",
      "address_1": "3500 Corporate Pkwy",
      "reason_for_recall": "Breakage of the endoscope's insertion tube bending section during surgical procedures.",
      "address_2": "PO Box 610",
      "product_quantity": "1062",
      "code_info": "All serial numbers",
      "center_classification_date": "20180720",
      "distribution_pattern": "US Nationwide. Canada and Mexico",
      "state": "PA",
      "product_description": "Uretero-reno fiberscope URF-P6",
      "report_date": "20180801",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Olympus Corporation of the Americas",
      "recall_number": "Z-2519-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79701",
      "termination_date": "20191204",
      "recall_initiation_date": "20180117",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}