{
  "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": "Covington",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80150",
      "recalling_firm": "C.R. Bard, Inc.",
      "address_1": "8195 Industrial Blvd NE",
      "address_2": "N/A",
      "postal_code": "30014-1497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL, NY, MN and TX  Canada, Japan and Taiwan",
      "recall_number": "Z-2064-2018",
      "product_description": "Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr.  Rx (01267522)",
      "product_quantity": "N/A",
      "reason_for_recall": "Foley Catheter with Incorrect Retainer Cap Print",
      "recall_initiation_date": "20171213",
      "center_classification_date": "20180606",
      "termination_date": "20201214",
      "report_date": "20180613",
      "code_info": "Catalog # 01267522 Lot #'s: NGBR0383 and NGBR2129"
    }
  ]
}