{
  "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": "75013",
      "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": "US Distribution",
      "recall_number": "Z-1883-2017",
      "product_description": "SmartSite Add-On Bag Access Device, Model No. 10013365",
      "product_quantity": "384,923 units",
      "reason_for_recall": "CareFusion is recalling the SmartSite Add-On Bag Device due to reports of separation and/or leakages between the spike port and the drip chamber spike.  A separation  or leak can cause a delay of infusion, an interruption of infusion, exposure to  medication or hazardous infusates, or underinfusion.",
      "recall_initiation_date": "20161117",
      "center_classification_date": "20170427",
      "termination_date": "20181029",
      "report_date": "20170503",
      "code_info": "15055146  15055702  15056299  15056618  15065645  15075740  15076166  15076167  15076664  15076729  15077085  15085031  15085156  15086107  15095014  15095411  15106928  15116928  15125952  15126069  15127413  16015324  16015325  16015607  16025824  16025948  16027008  16035527  16036131"
    }
  ]
}