{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82970",
      "recalling_firm": "Becton Dickinson & Company",
      "address_1": "1 Becton Dr",
      "address_2": "N/A",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign: Canada",
      "recall_number": "Z-0049-2020",
      "product_description": "CareFusion MaxPlus Clear Needleless Connector. Intended for Positive Displacement Connector for needleless access to the IV line and/or IV catheter during IV therapy    Cat. No. MP1000-C",
      "product_quantity": "115,200",
      "reason_for_recall": "After disconnection of a luer, the valve of the connector remains recessed; not fully closing, either temporarily or  permanently. The risks of blood loss and air embolism exist if the valve remains permanently open and goes  undetected, especially in the neonate population.",
      "recall_initiation_date": "20190502",
      "center_classification_date": "20191007",
      "termination_date": "20211130",
      "report_date": "20191016",
      "code_info": "Lot Number: 18085990; Exp. Date: 15-Aug-2023  UDI: 10885403223228"
    }
  ]
}