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USA Medical, LLC recalls Diagnostic Kit SARS-cCo V Antigen Rapid Test
Recalled May 18, 2022 · FDA recall Z-1050-2022 · USA Medical
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. · FDA Class II
Units
2055 kits
Sold at
U.S. Nationwide distribution in the states of CA, FL, IN, MD, MO, NJ, OK, and TN.
Description
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.
Product
Diagnostic Kit SARS-cCo V Antigen Rapid Test
Manufacturer(s)
USA Medical, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →