{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Covington",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93679",
      "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": "US",
      "recall_number": "Z-0797-2024",
      "product_description": "Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit\", 12Fr., 48in Long, REF EN0046120",
      "product_quantity": "26100 units",
      "reason_for_recall": "BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.",
      "recall_initiation_date": "20231220",
      "center_classification_date": "20240125",
      "report_date": "20240131",
      "code_info": "UDI/DI 00801741113239, Lot/Serial Numbers:  NGDT1998, NGDZ3287, NGEU0889, NGEU2134, NGEV2411, NGEW2655, NGEY1506, NGEZ0664, NGFN4265, NGFU4024, NGFV3514, NGFW1857, NGFX0168, NGFX2645, NGGQ8458, NGGR2705, NGGX4777"
    }
  ]
}