{
  "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",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83155",
      "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": "US Nationwide Distribution -   AZ  CA  CT  FL  GA  IL  KY  LA  MA  MD  MI  MN  MO  NJ  NY  OH  OK  OR  PA  TX  UT  VA  WA  WI  WV and PR. Worldwide foreign distribution.",
      "recall_number": "Z-2150-2019",
      "product_description": "Human Assayed Multi-Sera Level 2, Model NO. HN1530    Product Usage:  This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Human Assayed Multi-sera is for the control of accuracy.",
      "product_quantity": "149 (US)",
      "reason_for_recall": "The RX Series control target and range value for ALT (Tris buffer without P5P 37C), Bicarbonate and Gamma-GT has been incorrectly assigned in specific lots of the Human Assayed Multi-Sera Controls.",
      "recall_initiation_date": "20190611",
      "center_classification_date": "20190806",
      "termination_date": "20200515",
      "report_date": "20190814",
      "code_info": "1306UN, 1308UN, 1309UN"
    }
  ]
}