Lusys Laboratories, Inc. recalls Luscient Diagnostics 2nd Generation of COVID-19 Viral Antige
Recalled Product
Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For all mutant variety Cat: I-114(Nasal Swab Test)
Hazard / Issue
COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are not authorized, cleared, or approved for marketing and/or distribution in the U.S.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Part Number: I-114(N) Lot Numbers: All Lots due to not having an authorized Emergency Use Authorization (EUA)
View official government recall
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