{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "30085",
      "product_res_number": "Z-0090-04",
      "event_date_initiated": "2003-09-19",
      "event_date_posted": "2003-11-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-03-30",
      "res_event_number": "27562",
      "product_code": "CDZ",
      "product_description": "Device to determine quantitative total testosterone in human serum",
      "code_info": "Lots: 0307042, 0308019, and 0308020 Catalog #: 25000009",
      "firm_fei_number": "3003355251",
      "recalling_firm": "Qualigen Inc",
      "address_1": "2042 Corte Del Nogal",
      "city": "Carlsbad",
      "state": "CA",
      "postal_code": "92009-1438",
      "additional_info_contact": "Dorothy Deinzer\n760-918-9165",
      "reason_for_recall": "Kits may produce results that are falsely elevated.",
      "root_cause_description": "Other",
      "action": "All customers who received any one of the three lots have been faxed a removal letter starting 09/24/03. Certified or Airborne letter sent on 09/29/03.",
      "product_quantity": "81 Kits",
      "distribution_pattern": "Nationwide and Switzerland.",
      "openfda": {
        "k_number": [
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        "device_name": "Radioimmunoassay, Testosterones And Dihydrotestosterone",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.1680",
        "device_class": "1"
      }
    }
  ]
}