{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Waukegan",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90955",
      "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": "nationwide and Canada",
      "recall_number": "Z-0185-2023",
      "product_description": "Cardinal Health GEL PACK REUSABLE, EXTRA SMALL, Cat. 61115",
      "product_quantity": "1915308 units",
      "reason_for_recall": "Users are being informed that the product should not be used on infants/neonates. A caution statement will be added to the labeling stating:  Not for use on  Infants/Neonates .",
      "recall_initiation_date": "20220928",
      "center_classification_date": "20221107",
      "report_date": "20221116",
      "code_info": "All lots"
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}