{
  "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": [
    {
      "country": "United States",
      "city": "Montvale",
      "address_1": "3 Paragon Dr",
      "reason_for_recall": "The video cytoscopes lack 510(k) premarket notification clearance.",
      "address_2": "",
      "product_quantity": "24",
      "code_info": "Serial number: J110097  J110101  G110053  G110051  G110052  G110054  G110015  G110084  H110086  H110088  J110062  G110016  G110039  G110048  G110049  G110038  J110061  G110021  J110078  G110056  G110057  G110073  G110037  G110058",
      "center_classification_date": "20180214",
      "distribution_pattern": "Distributed in 8 states: CA, IL, MD, MI, ND, NH, NY, SD, and Guam.",
      "state": "NJ",
      "product_description": "Video Cystoscope models ECY-1570 and ECY-1570K",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Pentax of America Inc",
      "recall_number": "Z-0615-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79131",
      "termination_date": "20190722",
      "more_code_info": "",
      "recall_initiation_date": "20170713",
      "postal_code": "07645-1782",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}