{
  "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": "2026-04-15",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Franklin Lakes",
      "address_1": "1 Becton Dr",
      "reason_for_recall": "Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.",
      "address_2": "",
      "product_quantity": "6,720 units",
      "code_info": "Lot Number: 8337721  Exp. 30-Nov-2021  UDI: 382903835362",
      "center_classification_date": "20190603",
      "distribution_pattern": "US distribution to one distributor in VA.",
      "state": "NJ",
      "product_description": "BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system   Catalog Number: 383536",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Company",
      "recall_number": "Z-1710-2019",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "82330",
      "termination_date": "20200521",
      "more_code_info": "",
      "recall_initiation_date": "20190301",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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