{
  "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": [
    {
      "country": "United States",
      "city": "Northbrook",
      "address_1": "4088 Commercial Ave",
      "reason_for_recall": "Potential for a false-negative result.",
      "address_2": "",
      "product_quantity": "165",
      "code_info": "050620026A and 072120026B,",
      "center_classification_date": "20210702",
      "distribution_pattern": "Worldwide distribution - US Nationwide including in the states of AL, AZ, CA, CO, CT, DE, DC, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, NE, NV, NH, NJ, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA and VT. The countries of Austria, Chile, France, Germany, Greece, Italy, Japan, Kuwait, Netherlands, Spain, Thailand, Turkey, and United Kingdom.",
      "state": "IL",
      "product_description": "Verigene Gram Negative Blood Culture Nucleic Acid Test v2 (BC-GNv2) Model Number: 20-006-026",
      "report_date": "20210714",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Luminex Corporation",
      "recall_number": "Z-2011-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "88137",
      "more_code_info": "",
      "recall_initiation_date": "20201030",
      "postal_code": "60062-1829",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}