{
  "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": "Burnaby",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73225",
      "recalling_firm": "Novadaq Technologies Inc.",
      "address_1": "8329 Eastlake Dr Unit 101",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - Nationwide Distribution including Puerto Rico and to the countries of : Bangladesh, Canada, Hong Kong, India, and Israel.",
      "recall_number": "Z-1032-2016",
      "product_description": "PINPOINT Endoscopic Fluorescence Imaging System",
      "product_quantity": "110 units",
      "reason_for_recall": "It has been determined that the PINPOINT Operator's Manual does not contain validated parameters for gravity-cycle autoclave sterilization of the PINPOINT laparoscopes and light guide cable in the reprocessing tray.",
      "recall_initiation_date": "20160129",
      "center_classification_date": "20160302",
      "termination_date": "20161103",
      "report_date": "20160309",
      "code_info": "Rev. J, Rev. K, Rev. L and Rev. M    Model Number : PC9000"
    }
  ]
}