{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69054",
      "recalling_firm": "B. Braun Medical, Inc.",
      "address_1": "901 Marcon Blvd",
      "address_2": "N/A",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the state of  Missouri.",
      "recall_number": "Z-2655-2014",
      "product_description": "B.Braun Accuflo 100ML/H 100ML Elastomeric Infusion Device.    AccuFlo devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications.",
      "product_quantity": "8,640 units",
      "reason_for_recall": "The primary packaging label (inner pouch label) indicates that the package contents are Catalog Item: CT-1000-250, while the secondary packaging label (outer carton label) indicates the contents are CT-1000-100. The actual contents  are a CT-1000-100.",
      "recall_initiation_date": "20140806",
      "center_classification_date": "20140916",
      "termination_date": "20150129",
      "report_date": "20140924",
      "code_info": "Lot Number: 4A1125F111",
      "more_code_info": ""
    }
  ]
}