By Adam Sabes
Published 16 hours ago
The Food and Drug Administration announced Wednesday that a healthcare >company has recalled 45,500 COVID-19 rapid tests due to a "high number
of false positive reports."
Pharmaceutical company Celltrion USA announced on Feb. 28 it is
recalling specific lots of the DiaTrust COVID-19 Ag Rapid Test due to
the high number of false-positive reports, an FDA recall webpage read
The FDA says that a false-positive test result can lead to a delay in
"the correct diagnosis and treatment for the actual cause of a person's >illness."
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