{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Sandy",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94896",
      "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": "US: IL OUS: N/A0",
      "recall_number": "Z-2458-2024",
      "product_description": "BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25 mm) 63 mL/min, Rx Only. BD Insyte Autoguard BC Shielded IV Catheter is intended to be inserted into a patient's peripheral vascular system for short term use to sample blood, monitor blood pressure, or administer fluids.",
      "product_quantity": "26,400 units",
      "reason_for_recall": "Catheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.",
      "recall_initiation_date": "20240626",
      "center_classification_date": "20240731",
      "report_date": "20240807",
      "code_info": "Lot # 4127714/ UDI-DI: 00382903825332"
    }
  ]
}