{
  "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": "2026-04-22",
    "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": "65993",
      "recalling_firm": "B. Braun Medical, Inc.",
      "address_1": "901 Marcon Boulevard",
      "address_2": "N/A",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of FL, NY, NJ, and TX.",
      "recall_number": "Z-2166-2013",
      "product_description": "Outlook Safety Infusion System Burette Set.    For intravenous fluid administration.",
      "product_quantity": "900",
      "reason_for_recall": "Reports were received of an incorrectly assembled Outlook Safety Infusion System Burette Set (Product Code 375038), and the investigation determined that one of the ULTRASITE injection sites and corresponding low pressure backcheck valve was assembled upside down.",
      "recall_initiation_date": "20130805",
      "center_classification_date": "20130906",
      "termination_date": "20140903",
      "report_date": "20130918",
      "code_info": "Catelog Number 375038, Lot Number 0061317318, Expiration Date: 04/30/2016",
      "more_code_info": ""
    }
  ]
}