{
  "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": "68608",
      "recalling_firm": "CareFusion 303, Inc.",
      "address_1": "10020 Pacific Mesa Blvd",
      "address_2": "",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of FL, NM, WA, WI, and TX.",
      "recall_number": "Z-2025-2014",
      "product_description": "SmartSite Low Sorbing Infusion Set, Model Codes: 10014855A, 10015861A,   10061661A       14035457  14035485  14046894  14035458",
      "product_quantity": "5,600 units",
      "reason_for_recall": "CareFusion is recalling the SmartSite Low Sorbing Infusion Set because they were assembled with a drip chamber that consist of a 15 micron filter.  The Directions For Use did not indicate that the drip chamber has a 15 micron filter and it does not provide the instruction that the set should not be used with blood administration due to the potential for occluding the 15 micron filter in the drip c",
      "recall_initiation_date": "20140617",
      "center_classification_date": "20140709",
      "termination_date": "20160920",
      "report_date": "20140716",
      "code_info": "Lot No.  14035485  14046894  14035458  14035457",
      "more_code_info": ""
    }
  ]
}