FDAApril 9, 2021device

For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Antigen *** SARS-CoV-2 Antigen Rapid Qualitative Test *** REF BT1309

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

The hazard

Due to distributing test kits to customers who were not part of a clinical investigation.

What to do

FDA enforcement status: Ongoing

Brands named

innova medicalinnova

Recall history

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

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