{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Waukegan",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87145",
      "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": "Letter",
      "distribution_pattern": "Global Distribution.  US Nationwide.",
      "recall_number": "Z-1082-2021",
      "product_description": "Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K",
      "product_quantity": "137,346 kits",
      "reason_for_recall": "Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.",
      "recall_initiation_date": "20210107",
      "center_classification_date": "20210205",
      "termination_date": "20240214",
      "report_date": "20210217",
      "code_info": "Lots: 916197X  916881X  919683X  920354X  924620X  928728X  931205X"
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}