{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Fresno",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91321",
      "recalling_firm": "Universal Meditech Inc.",
      "address_1": "1320 E Fortune Avenue, Suite 102",
      "address_2": "N/A",
      "postal_code": "93725",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of CA, and TX.",
      "recall_number": "Z-0929-2023",
      "product_description": "Products are labeled as:    Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1 KIT      Green and white box under the brand DiagnosUS,     and,     White box without brand name labeled as \"SARS -COV-2 ANTIGEN DEVELOPMENT  MADE IN USA  ORAL SWAB TESTING",
      "product_quantity": "56,300 kits",
      "reason_for_recall": "Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market approval, clearance or Emergency Use Authorization.",
      "recall_initiation_date": "20221128",
      "center_classification_date": "20230127",
      "report_date": "20230208",
      "code_info": "Model Number: 550-10 UDI Code: None Lot Numbers: UL-AG-2111-01-Q UL-AG-2111-02-Q UL-AG-2110-05-Q UL-AG-2112-02-Q UL-AG-2110-03-Q UL-AG-2110-04-Q"
    }
  ]
}