{
  "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": "85208",
      "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": "US Nationwide",
      "recall_number": "Z-1763-2020",
      "product_description": "Olympus Pleuravideoscope, Model LTF-240",
      "product_quantity": "265 total",
      "reason_for_recall": "There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models.  Updated Operations Manuals are being provided.",
      "recall_initiation_date": "20200323",
      "center_classification_date": "20200422",
      "termination_date": "20211130",
      "report_date": "20200429",
      "code_info": "All Serial numbers"
    }
  ]
}