{
  "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": [
    {
      "country": "United States",
      "city": "Franklin Lakes",
      "address_1": "1 Becton Dr",
      "reason_for_recall": "Increased amount of residual blood present on the top of stopper well after venipuncture",
      "address_2": "",
      "product_quantity": "1,976,000 tubes",
      "code_info": "All Lot Numbers  Expiration Dates: November 30, 2017 - July 31, 2018    UDI No.:  50382903650434  50382903650441  50382903650458  50382903650472",
      "center_classification_date": "20180326",
      "distribution_pattern": "USA (nationwide)",
      "state": "NJ",
      "product_description": "BD Vacutainer¿ Barricor\" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 365043, 365044, 365045 & 365047      Used to collect, separate, process, transport and store venous blood samples for use in chemistry determinations, therapeutic drug monitoring and zinc testing in plasma for in vitro diagnostic use.",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Company",
      "recall_number": "Z-1180-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78909",
      "termination_date": "20190204",
      "more_code_info": "",
      "recall_initiation_date": "20170918",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}