{
  "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": "2026-06-17",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Crumlin",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83175",
      "recalling_firm": "Randox Laboratories, Limited",
      "address_1": "Ardmore; 55 The Diamond Road",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to CA  CT  MA  MD  MO  NC  NJ  NY  OH  PA  UT  WV   and PR. Worldwide foreign distribution.",
      "recall_number": "Z-2083-2019",
      "product_description": "RX Daytona, Model Nos. RX4040 and RX4041",
      "product_quantity": "3",
      "reason_for_recall": "There was a report of a malfunction with the sensor which resulted in an increase of temperature leading to melting of internal wires and scorch damage to the internal structure of the instrument.",
      "recall_initiation_date": "20190624",
      "center_classification_date": "20190725",
      "termination_date": "20200521",
      "report_date": "20190731",
      "code_info": "All serial numbers"
    }
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}