{
  "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": {
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      "city": "Waukegan",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
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      "recalling_firm": "Cardinal Health 200, LLC",
      "address_1": "3651 Birchwood Dr",
      "address_2": "",
      "postal_code": "60085-8337",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-1690-2023",
      "product_description": "Presource Kit, SMA21LPUHJ GYN Laparoscopy Pack.      Convenience kit used for Laparoscopic surgery",
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      "reason_for_recall": "Inadvertently released for distibution without sterility assurance.",
      "recall_initiation_date": "20230406",
      "center_classification_date": "20230606",
      "report_date": "20230614",
      "code_info": "Catalog Number: SMA21LPUHJ; Lot Number: 019693",
      "more_code_info": ""
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}