Two more rapid COVID-19 test kits have been recalled, one because it shows a “high number of false positives.” According to the U.S. Food and Drug Administration, the SD Biosensor Standard Q COVID-19 ...

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 ...

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. (WKBN) — Some COVID-19 home and rapid tests ...

(WKBN) — Some COVID-19 home and rapid tests have been recalled due to the potential for false-positive results. Celltrion USA recalled specific lots of the DiaTrust COVID-19 Ag Rapid Test due to many ...

The recalls were classified as class I recalls, the most serious type. Here are the four recalls, starting with the most recent: 1. Celltrion USA recalled 45,500 units of its DiaTrust COVID-19 Ag ...

(WKBN) — Some COVID-19 home and rapid tests have been recalled due to the potential for false-positive results. Celltrion USA recalled specific lots of the DiaTrust COVID-19 Ag Rapid Test due to many ...

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. Some COVID-19 home and rapid tests have been ...