FDAApril 4, 2022device

Diagnostic Kit SARS-cCo V Antigen Rapid Test

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

The hazard

COVID-19/SARS-CoV-2 Antigen Tests did not receive FDA Emergency Use Authorization, nor were the tests cleared or approved to be commercially distributed.

What to do

FDA enforcement status: Ongoing

Brands named

usa medicalusa

Recall history

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

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