{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87739",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - United States distribution and the countries of Canada, Korea, and Norway.",
      "recall_number": "Z-1684-2021",
      "product_description": "Gambro Cartridge Blood Set, Product Code 101025 - Product Usage: intended for single use in a hemodialysis treatment using the Phoenix Dialysis Delivery Systems.",
      "product_quantity": "17,487 units",
      "reason_for_recall": "There is a potential leak between the venous patient connector and patient's hemodialysis access.",
      "recall_initiation_date": "20210414",
      "center_classification_date": "20210526",
      "termination_date": "20240510",
      "report_date": "20210602",
      "code_info": "Product Code: 101025; Lot 1000276191, UDI: 37332414007837"
    }
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}