{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93074",
      "recalling_firm": "B. Braun Medical, Inc.",
      "address_1": "901 Marcon Blvd",
      "address_2": "",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada and Singapore.",
      "recall_number": "Z-0131-2024",
      "product_description": "30 ML 2PORT BURETTE ASSEMBLY, Article No. 7A3950, used in a contrast management system.",
      "product_quantity": "350 units",
      "reason_for_recall": "Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication.  There is also the potential for life-threatening situations to occur requiring additional medical intervention.",
      "recall_initiation_date": "20230926",
      "center_classification_date": "20231103",
      "report_date": "20231115",
      "code_info": "UDI-DI: N/A  Lots 0061766049",
      "more_code_info": ""
    }
  ]
}