{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Montvale",
      "address_1": "3 Paragon Dr",
      "reason_for_recall": "Pentax America Inc. is recalling various bronchoscopes which contain an incorrect Operation and Reprocessing IFUS.",
      "address_2": "",
      "product_quantity": "1719 units",
      "code_info": "EB-1170K; EB-1570K; EB-1575K; EB=1970K; EB-1970TK; EB-1975K",
      "center_classification_date": "20160922",
      "distribution_pattern": "Nationwide Distribution",
      "state": "NJ",
      "product_description": "Pentax Video Bronchoscope   Designed to be used with a Pentax Video Processor (including light source), documentation equipment, video monitor, endo-therapy accessories (such as biopsy forceps) and other ancillary equipment for endoscopy and endoscopic surgery within the airways and tracheobronchial tree.",
      "report_date": "20160928",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Pentax of America Inc",
      "recall_number": "Z-2875-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74954",
      "termination_date": "20171221",
      "more_code_info": "",
      "recall_initiation_date": "20160531",
      "postal_code": "07645-1782",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}