{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83191",
      "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": "U.S.: VA, DC, CA, FL, SC, MD, DE, PA, NC, WA, GA, TX, NV.     No foreign (OUS) distribution.",
      "recall_number": "Z-0030-2020",
      "product_description": "L5C4531 X1  Integrated APD Set with Cassette 3-Prong  Sterile, nonpyrogenic fluid path. Sterilized by ethylene oxide.",
      "product_quantity": "8640 eaches",
      "reason_for_recall": "Potential presence of leaks from the cassettes, which may be present due to an incomplete seal of the sheeting to the cassette. A leaking cassette could lead to contamination of the sterile fluid path with micro-organisms. This may predispose the patient to peritonitis.",
      "recall_initiation_date": "20181010",
      "center_classification_date": "20191003",
      "termination_date": "20200722",
      "report_date": "20191009",
      "code_info": "Lot Number H18D22030"
    }
  ]
}