{
  "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": [
    {
      "status": "Terminated",
      "city": "South San Francisco",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88869",
      "recalling_firm": "BioCheck, Inc.",
      "address_1": "425 Eccles Ave",
      "address_2": "N/A",
      "postal_code": "94080-1902",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of: MI, FL, NJ, OH, CA; and OUS (foreign) distribution to countries of: Spain, Taiwan and Nigeria",
      "recall_number": "Z-0214-2022",
      "product_description": "T4 EIA Kit, Cat No: BC-1007, Store at 2-8C, For in vitro diagnostic use only  This product s intended use is  For the quantitative determination of total thyroxine (T4) concentration in human serum. The test is useful in the diagnosis and treatment of thyroid disorders.",
      "product_quantity": "314 kits",
      "reason_for_recall": "Immunoassay TEST Kit do not meet product shelf-life standards resulting in failed controls.",
      "recall_initiation_date": "20211014",
      "center_classification_date": "20211110",
      "termination_date": "20250214",
      "report_date": "20211117",
      "code_info": "Lot # RN-60831 or RN-60923",
      "more_code_info": ""
    }
  ]
}