Migo Trading recalls FLOWFLEX SARS-COV-2 Antigen Rapid Tests due to lack of emergency use authorization. The product has not been validated for intended use and may not provide accurate results.
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.
Migo Trading is recalling FLOWFLEX SARS-COV-2 Antigen Rapid Tests because they were not authorized for emergency use and have not been validated for the intended purpose. This means the tests might not work correctly for detecting the virus.
The product was not approved for emergency use by the manufacturer and has not been validated for the intended purpose. This means the test may not detect the virus correctly, leading to false negatives or positives.
Anyone who purchased the FLOWFLEX SARS-COV-2 Antigen Rapid Test (1 Test) from the listed lot codes between May 2023 and September 2023. People using these tests for virus detection are at risk of inaccurate results.
Check the product label for lot codes COV1080232 (expires 05/13/2023) or COV1095004 (expires 09/03/2023). The product is a single-test rapid antigen test for SARS-COV-2.
Look for lot codes COV1080232 or COV1095004 on the product label.
The product was not authorized for emergency use and has not been validated for the intended purpose, so it may not provide accurate results.
Check the product label for lot codes COV1080232 (expires 05/13/2023) or COV1095004 (expires 09/03/2023).
The recall record does not specify a remedy, so contact the manufacturer for guidance.
We’ve drafted a message you can send Migo Trading to request your refund or repair — edit it as you like.
Subject: Recall Z-0421-2022 — Migo Trading Migo Trading Hello, I own a Migo Trading that is covered by recall Z-0421-2022 from Migo Trading. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
