{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Waukegan",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91560",
      "recalling_firm": "Cardinal Health 200, LLC",
      "address_1": "3651 Birchwood Dr",
      "address_2": "N/A",
      "postal_code": "60085-8337",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US Nationwide distribution in the states of GA, PA.",
      "recall_number": "Z-1157-2023",
      "product_description": "Cardinal Health Presource Packs IV START KIT- Intended for IV access device  CATALOG #: 01-5798B",
      "product_quantity": "4560 EA",
      "reason_for_recall": "Presource Kits contains the ICU MicroClave Clear  Connector due to a manufacturing defect there is a gap between the connectors top and bottom housings which  may lead to fluid leaks and loss of fluid path integrity",
      "recall_initiation_date": "20221118",
      "center_classification_date": "20230222",
      "report_date": "20230301",
      "code_info": "UDI-DI: 50195594577153(cs) 10195594577155(ea)  Lot Number: 816643 Exp. Date: 2/1/2025"
    }
  ]
}