{
  "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": "83886",
      "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": "Distributed to healthcare facilities in AR, FL, IL, NJ, TX, and WI.",
      "recall_number": "Z-0285-2020",
      "product_description": "13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI: 00801741066023    Power-Trialysis Short-Term Alphacurve Dialysis Catheter with a third internal umen for IV therapy, power injection of contrast media, and central venous pressure monitoring.",
      "product_quantity": "75 units",
      "reason_for_recall": "A portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.",
      "recall_initiation_date": "20190916",
      "center_classification_date": "20191105",
      "termination_date": "20200629",
      "report_date": "20191113",
      "code_info": "REDR0440"
    }
  ]
}