{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73008",
      "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": "US Distribution to:California and Utah.",
      "recall_number": "Z-1076-2016",
      "product_description": "BD Intelliport Medication Management System Sensor    The system is indicated for use by healthcare professionals in a hospital or medical center setting with patients who are receiving manually administered bolus intravenous injections as part of their care to facilitate documentation of the medications.",
      "product_quantity": "250 units",
      "reason_for_recall": "The sterility of the product cannot be assured. This may result in increased risk of infection.",
      "recall_initiation_date": "20151209",
      "center_classification_date": "20160308",
      "termination_date": "20170109",
      "report_date": "20160316",
      "code_info": "Catalog (Ref) # 516700 Lot numbers 5222723, 5251583 and 5253723."
    }
  ]
}