{
  "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": "Ongoing",
      "city": "Grapevine",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90098",
      "recalling_firm": "USA Medical, LLC",
      "address_1": "1220 Texan Trl Ste 205",
      "address_2": "N/A",
      "postal_code": "76051-4164",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of CA, FL, IN, MD, MO, NJ, OK, and TN.",
      "recall_number": "Z-1050-2022",
      "product_description": "Diagnostic Kit SARS-cCo V Antigen Rapid Test",
      "product_quantity": "2055 kits",
      "reason_for_recall": "COVID-19/SARS-CoV-2 Antigen Tests did not receive FDA Emergency Use Authorization, nor were the tests cleared or approved to be commercially distributed.",
      "recall_initiation_date": "20220404",
      "center_classification_date": "20220506",
      "report_date": "20220518",
      "code_info": "Catalog/Model/Part Number: None UDI Code:  None Lot Numbers:  Unknown/None"
    }
  ]
}