{
  "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": "66151",
      "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 in US: PA, OK, TX, FL, NC, CA, IN, WI",
      "recall_number": "Z-2285-2013",
      "product_description": "SmartSite Low Sorbing Infusion Set, Model# 10015048.  Intravascular administration set.",
      "product_quantity": "15860 units",
      "reason_for_recall": "CareFusion is recalling the SmartSite Low Sorbing Infusion Set, Model# 10015048, because there is a potential for separation at the tubing sleeve below the drip chamber.",
      "recall_initiation_date": "20130830",
      "center_classification_date": "20130926",
      "termination_date": "20140416",
      "report_date": "20131002",
      "code_info": "Lot Numbers 13015883 and 13025342."
    }
  ]
}