{
  "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": "83015",
      "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": "US Nationwide Distribution and Internationally to: Canada and Bermuda.",
      "recall_number": "Z-1909-2019",
      "product_description": "REVACLEAR 400 Dialyzer, Product Code 114746L     Revaclear 300 and Revaclear 400 dialyzers are indicated for treatment of chronic and acute renal failure by hemodialysis.",
      "product_quantity": "65403 units",
      "reason_for_recall": "There is a potential presence of ruptured dialyzer fibers which may lead to a blood leak during treatment.",
      "recall_initiation_date": "20190531",
      "center_classification_date": "20190701",
      "termination_date": "20201005",
      "report_date": "20190710",
      "code_info": "UDI 07332414124076  Lot Numbers:  C419205101  C419205201  C419205301"
    }
  ]
}