{
  "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": "Ongoing",
      "city": "Sandy",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90972",
      "recalling_firm": "Becton Dickinson Infusion Therapy Systems Inc.",
      "address_1": "9450 S State St",
      "address_2": "N/A",
      "postal_code": "84070-3213",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: New York, Florida, Maryland, North Carolina, Virginia, Georgia, Rhode Island, New Jersey, Pennsylvania, Illinois, South Carolina, Maine, and Massachusetts.  O.U.S.: N/A",
      "recall_number": "Z-0174-2023",
      "product_description": "BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr)",
      "product_quantity": "56,080 units",
      "reason_for_recall": "During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded (leaving the needle tip exposed).",
      "recall_initiation_date": "20221012",
      "center_classification_date": "20221103",
      "report_date": "20221109",
      "code_info": "Catalog Number: 383516 UDI-DI Code: (01)00382903835164 Lot Number: 2168865"
    }
  ]
}