{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Crumlin",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83153",
      "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": "E-Mail",
      "distribution_pattern": "Domestic distribution to Arizona, Oregon, Washington, and West Virginia. Foreign distribution to Australia, Belarus, Canada, France, Germany, Ireland, Kenya, Korea, Lithuania, New Zealand, Nigeria, Oman, Russia, Singapore, South Africa, Sweden, Switzerland, Turkey, and UK.",
      "recall_number": "Z-2207-2019",
      "product_description": "Assayed Bovine Multi-Sera Level 1, Model No. AL1027",
      "product_quantity": "4 kits (US)",
      "reason_for_recall": "The firm is re-assigning the Mean of all Instruments target and range for Bile Acids (5th Generation Colorimetric) in the Assayed Bovine Multi-Sera Level 1 Control Lot 205SL.",
      "recall_initiation_date": "20190610",
      "center_classification_date": "20190807",
      "termination_date": "20200616",
      "report_date": "20190814",
      "code_info": "205SL"
    }
  ]
}