{
  "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": [
    {
      "country": "United States",
      "city": "Kearneysville",
      "address_1": "515 Industrial Blvd",
      "reason_for_recall": "The ACTH in Immunoassay Premium and Premium Plus quality control does not meet the quoted reconstituted stability claim in the product IFU.",
      "address_2": "",
      "product_quantity": "117 Kits",
      "code_info": "Catalog numbers:   IA2633 (Lots: 398703, 402366)  IA2638 (Lot 1666EC)  IA2639 (Lots: 1486EC, 1516EC, 1626EC)  IA2640 (Lots 1517EC, 1668EC)",
      "center_classification_date": "20180312",
      "distribution_pattern": "Distribution US nationwide.",
      "state": "WV",
      "product_description": "Immunoassay Premium Controls (3x4x5mL and 12x5mL packages)",
      "report_date": "20180321",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Randox Laboratories",
      "recall_number": "Z-0969-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79076",
      "termination_date": "20190329",
      "more_code_info": "",
      "recall_initiation_date": "20170811",
      "postal_code": "25430-2778",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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  ]
}