{
  "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": "N/A",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86827",
      "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": "US Nationwide distribution in the states of GA, NJ.",
      "recall_number": "Z-0547-2021",
      "product_description": "Randox Rx Series Mg - Product Usage: For the quantitative in vitro determination of Magnesium in serum, plasma and urine  Catalogue Number: MG8326",
      "product_quantity": "4 kits",
      "reason_for_recall": "Failing to meet the linearity performance claims  quoted on the kit inserts-The linearity is reduced by approximately -30% for Serum/ Plasma and -50% for Urine",
      "recall_initiation_date": "20201113",
      "center_classification_date": "20201208",
      "termination_date": "20210401",
      "report_date": "20201216",
      "code_info": "Lot Number: 539770 Exp. Date : 28 March 2022    UDI: 05055273209303"
    }
  ]
}