{
  "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": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66758",
      "recalling_firm": "CareFusion 303, Inc.",
      "address_1": "10020 Pacific Mesa Blvd",
      "address_2": "N/A",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-0435-2014",
      "product_description": "VersaSafe Extension Set, Model No. 21000M-007",
      "product_quantity": "3500 units",
      "reason_for_recall": "CareFusion is recalling the VersaSafe Extension Intravascular  Administration Set because it may have excessive adhesive  which will prevent the male spin collar to operate as intended.",
      "recall_initiation_date": "20131108",
      "center_classification_date": "20131203",
      "termination_date": "20140417",
      "report_date": "20131211",
      "code_info": "Lot No. 13066550"
    }
  ]
}