{
  "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": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84339",
      "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": "Nationwide",
      "recall_number": "Z-1409-2020",
      "product_description": "Revaclear Capillary Dialyzer 300, REF Revaclear 300 Product Code 114745L",
      "product_quantity": "101976 devices",
      "reason_for_recall": "There is the potential presence of particular matter in the header caps of ten lots the Revaclear 300 Dialyzer.",
      "recall_initiation_date": "20191115",
      "center_classification_date": "20200228",
      "termination_date": "20201120",
      "report_date": "20200311",
      "code_info": "UDI 07332414123055, Lot Numbers:  C419124901, C419125001, C419125101, C419125201, C419125401, C419125501, C419125601, C419125801, C419126001, C419126401"
    }
  ]
}