{
  "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": "2026-04-01",
    "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": "84733",
      "recalling_firm": "Cardinal Health",
      "address_1": "1350 Bridge Dr",
      "address_2": "N/A",
      "postal_code": "60085-6306",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution  US Nationwide including Puerto Rico and Guam, United Arab Emirates, Australia, Canada, Chile, Colombia, Costa Rica, Dominican Republic, Israel, Mexico, Oman, Panama, Philippines, and Saudi Arabia.",
      "recall_number": "Z-1032-2020",
      "product_description": "GOWN SURG LG W/TOWEL ST BACK, Item Code 9515",
      "product_quantity": "7,659,634 total units",
      "reason_for_recall": "The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.",
      "recall_initiation_date": "20200111",
      "center_classification_date": "20200205",
      "termination_date": "20230119",
      "report_date": "20200212",
      "code_info": "Lot Numbers: XXXXJXXX    Single-Sterile Lot Format: YYMRJXXX   Where:  YY   Last two digits of the year ( 18 or '19)   M   Month in alpha code    \" If made in 2018   o  J  for September    o  K  for October    o  L  for November OR    o  M  for December       \" If made in 2019, any value is affected   R   Product revision or suffix   P   Facility code is letter  J    XXX Sequential Number - Monthly reset     OR    Bulk Non-Sterile Lot Format: XXXYRPQ   Where:  XXX   Elapsed days of year   \" \" If made in 2018,  244  or greater is affected OR   \" \" If made in 2019, any value is affected; see below for year made identifier   Y   Last character of year gown was made (2018 or 2019)   R   Product Revision   P   Facility code is letter  J    Q   Plant shift identifier; this identifier was added during the affected time period and therefore older product may not contain this digit in the lot number"
    }
  ]
}