{
  "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-1532-2018",
      "product_description": "BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 mm x 305 mm 21G x ¿  x 12  Catalog 367344",
      "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": "7346627  7348974  7348975  7354740  7354743  7354745  7354764  8005556  8005557  8005814  8010735  8012910  8015923  8015925"
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