Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Diagnostic Kit SARS-cCo V Antigen Rapid Test Recalled by USA Medical, LLC Due to COVID-19/SARS-CoV-2 Antigen Tests did not receive FDA Emergency...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact USA Medical, LLC directly.
Affected Products
Diagnostic Kit SARS-cCo V Antigen Rapid Test
Quantity: 2055 kits
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About USA Medical, LLC
USA Medical, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report