{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Deerfield",
      "address_1": "1 Baxter Pkwy",
      "reason_for_recall": "Potential presence of particulate matter on the blood side of the dialyzer",
      "address_2": "",
      "product_quantity": "22,656 units",
      "code_info": "C416201601",
      "center_classification_date": "20161108",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and the countries of Canada and Mexico.",
      "state": "IL",
      "product_description": "GAMBRO Capillary Dialyzer, Polyflux(R) Revaclear MAX, STERILE, Product code 110634      Product Usage:  The Revaclear Max dialyzer is a single use device used for treatment of chronic and acute renal failure by hemodialysis.",
      "report_date": "20161116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corp.",
      "recall_number": "Z-0370-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75414",
      "termination_date": "20170819",
      "more_code_info": "",
      "recall_initiation_date": "20161012",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}