{
  "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": [
    {
      "country": "United States",
      "city": "Dublin",
      "address_1": "7000 Cardinal Pl",
      "reason_for_recall": "The double wrapping of this custom kit basin set is not supported by the current sterility assurance validation.",
      "address_2": "",
      "product_quantity": "182 packs",
      "code_info": "Product code: SOP22TJCLK  Lot numbers # 104405, 122793, and 987948",
      "center_classification_date": "20190109",
      "distribution_pattern": "US state of Florida",
      "state": "OH",
      "product_description": "Presource Kit Total Joint Pack containing a double-wrapped basin component.      Product Usage: This kit is used on patients undergoing joint replacement knee or hip.",
      "report_date": "20190116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cardinal Health Inc.",
      "recall_number": "Z-0702-2019",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "81756",
      "termination_date": "20191104",
      "more_code_info": "",
      "recall_initiation_date": "20181116",
      "postal_code": "43017-1091",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}