{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Covington",
      "address_1": "8195 Industrial Blvd NE",
      "reason_for_recall": "BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.",
      "address_2": "",
      "product_quantity": "23400 units",
      "code_info": "Lot numbers:  NGARX207, NGAX3462",
      "center_classification_date": "20180410",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "GA",
      "product_description": "Bard(R) Infant Feeding Tube, ENFit(TM), REF EN0036410     Product Usage:  BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for:   Decompression of stomach by suction or aspiration of gastric contents   Short-term administration of term tube feeding, lavage fluid and medications Feeding Tubes with the ENFit(TM) Connector are made of a smooth plastic with a two-eyed tube used for nasogastric feeding of neonates, infants and adults as well as diagnostic and therapeutic aspiration. These products are sold single-use, sterile. The Feeding Tube with the ENFit(TM) connector provides a way to reduce the risk of enteral device misconnections. The ENFit(TM) connector:   Addresses patient side connections between feeding tubes, administration sets, medication, flush and bolus feeding syringes, and other enteral devices. Does not allow connectivity with any other connector for any other clinical use.",
      "report_date": "20180418",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "C.R. Bard, Inc.",
      "recall_number": "Z-1355-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79507",
      "termination_date": "20190711",
      "more_code_info": "",
      "recall_initiation_date": "20180227",
      "postal_code": "30014-1497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}