{
  "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": "2026-08-20",
    "results": {
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  "results": [
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      "cfres_id": "190340",
      "product_res_number": "Z-0421-2022",
      "event_date_initiated": "2021-11-04",
      "event_date_created": "2021-12-27",
      "recall_status": "Open, Classified",
      "res_event_number": "89028",
      "product_code": "QKP",
      "product_description": "FLOWFLEX SARS-COV-2 Antigen Rapid Test (Self-Testing), 1 Test",
      "code_info": "UDI #: 6921756492427\n\nLot codes: \nCOV1080232 - Expiration date: 05/13/2023; \nCOV1095004 - Expiration date: 09/03/2023",
      "firm_fei_number": "3018125969",
      "recalling_firm": "Migo Trading LLC",
      "address_1": "831 Laca St",
      "city": "Dayton",
      "state": "NV",
      "postal_code": "89403-6394",
      "additional_info_contact": "Michael Gothelf\n973-810-7444",
      "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.",
      "root_cause_description": "No Marketing Application",
      "action": "On November 4, 2021, Migo Trading issued URGENT MEDICAL DEVICE RECALL notices and response forms dated November 1, 2021 to customers via email.  \n\nActions to be taken by the Customer/User:\n- Please inspect stock and quarantine impacted product.\n- Please discard any available inventory in your possession or by your customer s possession.\n- If you have used these devices to determine your SARS-CoV-2 infection status, it is possible that your test result is incorrect. It is recommended that you obtain a confirmatory test to determine your SARS-CoV-2 infection status.\n- Complete and return the attached response form via email at info@migotrading.com",
      "product_quantity": "200,100 units",
      "distribution_pattern": "NY",
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        "device_name": "Coronavirus Antigen Detection Test System.",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
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    }
  ]
}