{
  "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": "2026-04-15",
    "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": "70858",
      "recalling_firm": "Olympus America Inc.",
      "address_1": "3500 Corporate Pkwy.",
      "address_2": "P.O. Box 610",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and countries of: Canada and Mexico.",
      "recall_number": "Z-2807-2015",
      "product_description": "EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V.     This instrument has been designed to be used with an Olympus video system center, light source, documentation equipment, monitors,  EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery within the duodenum.",
      "product_quantity": "6109",
      "reason_for_recall": "New and validated reprocessing procedures have been issued for the Olympus TJF-Q180V duodenoscope (\"TJF-Q180V\"), consisting of revised manual cleaning and high level disinfection procedures.",
      "recall_initiation_date": "20150326",
      "center_classification_date": "20150922",
      "termination_date": "20170201",
      "report_date": "20150930",
      "code_info": "Model:  TJF-Q180V, all sold units"
    }
  ]
}