{
  "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": [
    {
      "status": "Terminated",
      "city": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77513",
      "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": "Nationwide Distribution",
      "recall_number": "Z-2753-2017",
      "product_description": "BD 3ml Syringer Luer-Lok Tip  Catalog #309604  The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection",
      "product_quantity": "1,528,000 units",
      "reason_for_recall": "BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required.",
      "recall_initiation_date": "20160916",
      "center_classification_date": "20170719",
      "termination_date": "20180320",
      "report_date": "20170726",
      "code_info": "6061746 2021-02  6082982 2021-02  6089821 2021-03  6117858 2021-04  6117863 2021-04  6117889 2021-04  6117891 2021-04  6146962 2021-04  6173697 2021-05  6173767 2021-06  6173779 2021-06  6208614 2021-07"
    }
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}