{
  "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": "Crumlin (North)",
      "state": "",
      "country": "Ireland",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83592",
      "recalling_firm": "Randox Laboratories Ltd.",
      "address_1": "55 Diamond Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution including the states of IN, WV.",
      "recall_number": "Z-2557-2019",
      "product_description": "Randox Urinalysis Control   Level 2 (IVD)   Ref: UC5034 - Product Usage: Product is intended for in vitro diagnostic use in the quality control of urine test strips.",
      "product_quantity": "1 kit",
      "reason_for_recall": "Analyte range for Leukocytes for use with the Siemens Multistix method is incorrect. The range was corrected to NEGATIVE to 3+.",
      "recall_initiation_date": "20190725",
      "center_classification_date": "20190923",
      "termination_date": "20201203",
      "report_date": "20191002",
      "code_info": "Lot: 1020UC  Exp. Date: 28 May 2020",
      "more_code_info": ""
    }
  ]
}