{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northbrook",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90122",
      "recalling_firm": "Luminex Corporation",
      "address_1": "4088 Commercial Ave",
      "address_2": "N/A",
      "postal_code": "60062-1829",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Kuwait, Austria, France, Greece, Kuwait, Turkey.",
      "recall_number": "Z-1334-2022",
      "product_description": "Verigene CDF Nucleic Acid Test, Part No. 30-002-22",
      "product_quantity": "296 units",
      "reason_for_recall": "There is a potential for false negative results using VERIGENE CDF Stool PREP KIT and VERIGENE EP Stool PREP KIT due to hydrophobic characteristics of the swab.",
      "recall_initiation_date": "20220617",
      "center_classification_date": "20220706",
      "report_date": "20220713",
      "code_info": "UDI 00840487101735 Luminex Lot Number 042021022D, FLOQ Swab Lot Numbers:  2100856, 2032870;  Luminex Lot Number 071321022F, FLOQ Swab Lot Numbers:  2100856, 2107946;  Luminex Lot Number 100421022A, FLOQ Swab Lot Numbers:  2110850;  Luminex Lot Number 110221022E, FLOQ Swab Lot Numbers:  2107946.",
      "more_code_info": ""
    }
  ]
}