{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Breinigsville",
      "address_1": "200 Boulder Dr",
      "reason_for_recall": "B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector due to a potential for some blisters to be punctured resulting in a compromised sterility barrier.",
      "address_2": "",
      "product_quantity": "417,600 units",
      "code_info": "Lot #   1240156001, 1240156002, 1240156003, 1240156004, 1370249001, 1370251101, 1370257101, 1370259201, 1370268401, 1370270401, 1370273801, 1470311101, and 1570315301",
      "center_classification_date": "20170523",
      "distribution_pattern": "United States Nationwide distribution",
      "state": "PA",
      "product_description": "CytoGuard Closed Luer Connector, Intravenous access 2 cartons of 50 units each (100 units per case)",
      "report_date": "20170531",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "B Braun Medical Inc",
      "recall_number": "Z-2155-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77112",
      "termination_date": "20180202",
      "more_code_info": "",
      "recall_initiation_date": "20170410",
      "postal_code": "18031-1532",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}