{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northbrook",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94970",
      "recalling_firm": "Luminex Corporation",
      "address_1": "4088 Commercial Ave",
      "address_2": "",
      "postal_code": "60062-1829",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution including in the states of AZ, CA, CO, DE, FL, GA, IA, IL, KY, MD, MI, MN, MO, MS, NE, NV, OH, OK, SC, TN, TX, VA, VT, WA, WV.",
      "recall_number": "Z-2533-2024",
      "product_description": "Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test",
      "product_quantity": "1,100 kits",
      "reason_for_recall": "Potential for defective test cartridges which may result in false positive results for the Staphylococcus lugdunensis and Enterococcus faecium targets.",
      "recall_initiation_date": "20240620",
      "center_classification_date": "20240808",
      "report_date": "20240814",
      "code_info": "GTIN Number: 00840487101575; Catalog Number: 20-006-018; Lot Number: 031824018A; Expiration Date: 09/16/2024",
      "more_code_info": ""
    }
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}