{
  "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": "Waukegan",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74706",
      "recalling_firm": "Cardinal Health",
      "address_1": "1300 Waukegan Rd",
      "address_2": "N/A",
      "postal_code": "60085-6724",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) and Canada.",
      "recall_number": "Z-2713-2016",
      "product_description": "The 9025TRU Arterial Blood Gas (ABG) Kit is used to obtain arterial blood sampling for pH, Blood Gas, Electrolyte and Metabolite Analysis.",
      "product_quantity": "Lot #884993 -16,000 units, Lot #903136 -1,900 units and Lot #903137 - 300 units.",
      "reason_for_recall": "Arterial Blood Gas (ABG) Kit- Missing Safety Component. The ABG Kit(s) have been identified as missing the locking clasp component. CareFusion/BD has identified a potential customer/user safety risk associated with the missing locking clasp component.",
      "recall_initiation_date": "20160627",
      "center_classification_date": "20160901",
      "termination_date": "20180302",
      "report_date": "20160907",
      "code_info": "Three (3) total lots (lot #884993, lot #903136 & lot #903137)."
    }
  ]
}