{
  "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": [
    {
      "country": "United States",
      "city": "Park City",
      "address_1": "1430  Waukegan Road",
      "reason_for_recall": "Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.",
      "address_2": "Attn V. Mueller Qa",
      "product_quantity": "4,571 Kits total",
      "code_info": "Catalog Number: PO24THGWG01; Lots: 966051, 970753",
      "center_classification_date": "20130503",
      "distribution_pattern": "Distributed in the states of AR, MS, SC, and TN.",
      "state": "IL",
      "product_description": "Presource PBDS, Total Hip, Kit, Circulator",
      "report_date": "20130515",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Cardinal Health, Medical Products & Services",
      "recall_number": "Z-1202-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64736",
      "termination_date": "20170412",
      "recall_initiation_date": "20130326",
      "postal_code": "60085",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}