{
  "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": [
    {
      "country": "United States",
      "city": "Franklin Lakes",
      "address_1": "1 Becton Dr",
      "reason_for_recall": "BD is conducting a recall of the BD Vacutainer 2.7mL Plus Citrate Blood Collection Tube due to extended Partial Thromboplastin Time (aPTT) test results reported in two customer complaints.",
      "address_2": "",
      "product_quantity": "2,944,700 units",
      "code_info": "Lot No. 2180434; Expiration Date: April 2013",
      "center_classification_date": "20130131",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Canada, India, Japan, Nepal, Malaysia, Singapore, Brazil, Costa Rica, and Virgin Islands.",
      "state": "NJ",
      "product_description": "BD Vacutainer Buffered Sodium Citrate (9NC) Plus Blood Collection Tubes; Sterile; IVD; REF 363083; 13 X 75 mm, 2.7 mL",
      "report_date": "20130206",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Company",
      "recall_number": "Z-0756-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64010",
      "termination_date": "20130906",
      "more_code_info": "",
      "recall_initiation_date": "20121112",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}