{
  "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": "Dayton",
      "state": "NV",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89028",
      "recalling_firm": "Migo Trading LLC",
      "address_1": "831 Laca St",
      "address_2": "",
      "postal_code": "89403-6394",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NY",
      "recall_number": "Z-0421-2022",
      "product_description": "FLOWFLEX SARS-COV-2 Antigen Rapid Test (Self-Testing), 1 Test",
      "product_quantity": "200,100 units",
      "reason_for_recall": "Devices are determined to be inconsistent with the firm's Emergency Use Authorization (EUA).  This product has not been authorized for emergency use and the test cannot be determined to be adequately validated for the stated intended use.",
      "recall_initiation_date": "20211104",
      "center_classification_date": "20211227",
      "report_date": "20220105",
      "code_info": "UDI #: 6921756492427  Lot codes:  COV1080232 - Expiration date: 05/13/2023;  COV1095004 - Expiration date: 09/03/2023",
      "more_code_info": ""
    }
  ]
}