The FDA revoked Johnson and Johnson’s emergency US authorization for the COVID vaccine.

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The Food and Drug Administration (FDA) announced it had revoked the emergency use authorization (EUA) of the COVID-19 Vaccine Janssen.

On May 22, Janssen Biotech, a unit of US healthcare giant Johnson & Johnson, requested the voluntary withdrawal of the EUA for this vaccine, the FDA noted.

https://www.thepharmaletter.com/in-brief/brief-fda-revokes-eua-for-covid-19-vaccine-janssen
https://www.fda.gov/vaccines-blood-biologics/coronavirus-covid-19-cber-regulated-biologics/janssen-covid-19-vaccine

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