{
  "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": "Lombard",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88478",
      "recalling_firm": "Thera Test Laboratories, Inc.",
      "address_1": "1120 N Du Page Ave",
      "address_2": "N/A",
      "postal_code": "60148-1247",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of California, Florida, Illinois, Indiana, North Carolina, and Texas.",
      "recall_number": "Z-2382-2021",
      "product_description": "EL-Anti-SARS-CoV-2 IgG Kit, Catalog #104-130. Submitted as EUA202128",
      "product_quantity": "19 kits",
      "reason_for_recall": "The cross-reactivity of the device may present an increased level of potential false positives. Submitted as EUA202128",
      "recall_initiation_date": "20201005",
      "center_classification_date": "20210827",
      "termination_date": "20220215",
      "report_date": "20210908",
      "code_info": "Lot numbers 05204351, exp. 5/1/2021, and 05204368, exp. 05/19/2021."
    }
  ]
}