{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Crumlin",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79035",
      "recalling_firm": "Randox Laboratories, Limited",
      "address_1": "Ardmore 55 The Diamond Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationally",
      "recall_number": "Z-0937-2018",
      "product_description": "Liquid Cardiac Control CQ5053",
      "product_quantity": "450 kits",
      "reason_for_recall": "Randox has confirmed that Troponin T and Troponin I in Liquid Cardiac quality control CQ5053 lot 4069CK does not meet the shelf-life claim in the product labelling. As the control may now fall outside the provided control ranges the product is to be recalled from the field.",
      "recall_initiation_date": "20170808",
      "center_classification_date": "20180309",
      "termination_date": "20180905",
      "report_date": "20180321",
      "code_info": "Lot 4069CK",
      "more_code_info": ""
    }
  ]
}