{
  "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": "88130",
      "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 AR, CA, CT, NY, OH, PA, TN, and TX",
      "recall_number": "Z-2099-2021",
      "product_description": "NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of NEFA  Catalog Number: FA115",
      "product_quantity": "71 kits US",
      "reason_for_recall": "Standard  packed within NEFA kit has been assigned incorrectly. Calibrating with the incorrect value will cause a positive shift of up to +8% with both quality controls and patient samples",
      "recall_initiation_date": "20210510",
      "center_classification_date": "20210720",
      "termination_date": "20211110",
      "report_date": "20210728",
      "code_info": "Batch Number: 544642  Exp. Date: 28th Nov 2022  GTIN: 05055273203066",
      "more_code_info": ""
    }
  ]
}