{
  "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": {
      "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": "76129",
      "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",
      "recall_number": "Z-1440-2017",
      "product_description": "Eclipse Hypodermic Needle",
      "product_quantity": "263 mm units",
      "reason_for_recall": "BD is initiating a Product Advisory for the Eclipse Hypodermic Needle because of safety complaints covering disengagement and needlestick injuries.",
      "recall_initiation_date": "20161220",
      "center_classification_date": "20170310",
      "termination_date": "20180420",
      "report_date": "20170322",
      "code_info": "N/A"
    }
  ]
}