{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Montvale",
      "address_1": "3 Paragon Dr",
      "reason_for_recall": "The Instructions for Use for the Pentax OF-B130 and OF-B194 Gas/Water Valve IFU if not followed carefully may cause a potential risk to health.",
      "address_2": "",
      "product_quantity": "98 units US; 1108 units OUS",
      "code_info": "Model No. OF-B130  OF-B194, all units.",
      "center_classification_date": "20140821",
      "distribution_pattern": "Worldwide Distribution - US Distribution including the states of CA, CO, IN, KS and ID., and the countries of Asia, Canada, Europe and Japan.",
      "state": "NJ",
      "product_description": "PENTAX Upper/Lower G.I. Endoscope  OF-B130 and OF-B194 Gas/Water Feeding Valve",
      "report_date": "20140827",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Pentax Medical Company",
      "recall_number": "Z-2290-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68753",
      "termination_date": "20150820",
      "more_code_info": "",
      "recall_initiation_date": "20140717",
      "postal_code": "07645-1782",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}