{
  "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": "Richmond",
      "state": "British Columbia",
      "country": "Canada",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69839",
      "recalling_firm": "Novadaq Technologies, Inc.",
      "address_1": "13155 Delf Place",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution to IA, LA, GA, MD, ID, FL, TN, OH, TX, NC, MA, KY, KS, WI, IN, SC, OR, CT, CA, WA, PA, OK, and PR.",
      "recall_number": "Z-0470-2015",
      "product_description": "Non-sterile drape",
      "product_quantity": "324 units",
      "reason_for_recall": "Non sterile-drape LUNA drape was inadvertently mislabeled with an additional contents sterile label.",
      "recall_initiation_date": "20141104",
      "center_classification_date": "20141126",
      "termination_date": "20151106",
      "report_date": "20141203",
      "code_info": "Kit Lot Numbers:  14082, 14091, 14104, 14106  Drape Lot Numbers:  D132712, D133102, D141022, D130282",
      "more_code_info": ""
    }
  ]
}