{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Crumlin (North)",
      "state": "",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81664",
      "recalling_firm": "Randox Laboratories Ltd.",
      "address_1": "55 Diamond Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of : IN, NJ, NY, TX and WV and internationally to Ireland.",
      "recall_number": "Z-0660-2019",
      "product_description": "SP CAL (LIQ), REF IT2692     This product is intended for in vitro diagnostic use with Randox Alpha-1-Antitrypsin, Alpha-1-Acid Glycoprotein, IgA, IgG and IgM assays that require sample predilution.",
      "product_quantity": "250 kits (32 kits US / 218 kits OUS)",
      "reason_for_recall": "Calibrator value sheets have been modified for  assigned value of Alpha-1-Acid-Glycoprotein (AGP), IgA and IgG to improve the alignment.  IgG measurement reference has also been corrected.",
      "recall_initiation_date": "20181119",
      "center_classification_date": "20181221",
      "termination_date": "20200423",
      "report_date": "20190102",
      "code_info": "05055273204049  Lot Number: 415879  Date of Expiry - 28 March 2019",
      "more_code_info": ""
    }
  ]
}