FDANovember 4, 2021device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

migo tradingmigo

UPCs

6921756492427

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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