{
  "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": "2026-04-08",
    "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": "79687",
      "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 (Nationwide) Canada, Kuwait, Guyana, Guatemala,  Taiwan, UK, Belgium, Sweden, Ireland, Israel, Spain, Switzerland and Lithuania",
      "recall_number": "Z-1533-2018",
      "product_description": "BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 x 19 mm x 305 mm 23G x ¿  x 12.  Catalog no 367364",
      "product_quantity": "N/A",
      "reason_for_recall": "Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.",
      "recall_initiation_date": "20180320",
      "center_classification_date": "20180426",
      "termination_date": "20200420",
      "report_date": "20180502",
      "code_info": "7348980"
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}