{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Franklin Lakes",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65322",
      "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-1923-2013",
      "product_description": "BD Vacutainer Multiple Sample and Direct Draw Luer Adapter  BD Franklin Lakes, NJ 07417 USA    A sterile non-invasive device used to connect venous access devices such as needles, blood collection sets, ad infusion sets to blood collection tubes.",
      "product_quantity": "37,906,400 units",
      "reason_for_recall": "BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood leakage and low draw volume.",
      "recall_initiation_date": "20130501",
      "center_classification_date": "20130807",
      "termination_date": "20151204",
      "report_date": "20130814",
      "code_info": "Marketing Status: Class II, 510K #  K991088  Device Listing Number:  D030347    Catalog number 367290, 367300 (CE), 368491, and 303380."
    }
  ]
}