Reported Jan 5, 2022 · Ongoing

FLOWFLEX SARS-COV-2 Antigen Rapid Test (Self-Testing), 1 Test

Migo Trading LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Migo Trading LLC · 831 Laca St · Dayton, NV · 89403-6394

Is this the product you have?

  • FLOWFLEX SARS-COV-2 Antigen Rapid Test (Self-Testing), 1 Test
Lot codes and dates
  • UDI #: 6921756492427
  • Lot codesCOV1080232 -
  • Expiration date05/13/2023
  • COV1095004 - Expiration date09/03/2023
Amount recalled
200,100 units

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:20 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.