{
  "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,
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  },
  "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-2749-2017",
      "product_description": "BD 3ml Syringe Luer-Lok\" Tip with BD PrecisionGlide\" Needle 23G x 1 (0.6mm x 25mm)  Catalog #309571  The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection",
      "product_quantity": "57600 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": "6117580 2021-03"
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}