{
  "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 III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82184",
      "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": "Letter",
      "distribution_pattern": "The products were distributed to the following US states: WV and Puerto Rico.",
      "recall_number": "Z-1106-2019",
      "product_description": "Immunoassay Premium Plus Controls, Model Numbers IA3109 and IA3112    Product Usage:  This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert",
      "product_quantity": "12",
      "reason_for_recall": "The target value for uptake is incorrect on the value sheet for an analyzer.  The target value for this analyzer is listed as 43.8%U and should be 39.4%U.",
      "recall_initiation_date": "20190207",
      "center_classification_date": "20190408",
      "termination_date": "20200608",
      "report_date": "20190417",
      "code_info": "Lot codes: 1714EC   430312   432364"
    }
  ]
}