{
  "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": "Crumlin (North)",
      "state": "N/A",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82400",
      "recalling_firm": "Randox Laboratories Ltd.",
      "address_1": "55 Diamond Road",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Product distributed to CA, DE, WV, and Puerto Rico.",
      "recall_number": "Z-1785-2019",
      "product_description": "Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053",
      "product_quantity": "11420 kits",
      "reason_for_recall": "Customers may observe a decrease in recovered concentration with regards to NTproBNP in the Liquid Cardiac Control lots identified, on the Siemens Dimension EXL LOCI.",
      "recall_initiation_date": "20190311",
      "center_classification_date": "20190614",
      "termination_date": "20200515",
      "report_date": "20190626",
      "code_info": "lots 4243CK, 4244CK, 4245CK."
    }
  ]
}