{
  "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,
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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-1531-2018",
      "product_description": "BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 mm x 305 mm  23G x ¿  x 12  (Catalog no 367342)",
      "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": "7354908  8005794  8005795  8005796  8010728  8010732  8012784  8012844  8012848  8018509  8019702"
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