The U.S. Food and Drug Administration (FDA) announced a recall for hot dog and burger buns made by Hostess Brands LLC over listeria and salmonella concerns.
A Food and Drug Administration (FDA) official said that emergency authorization for COVID vaccines in children under 12 could be expected by midwinter.
The U.S. Food and Drug Administration issued a new warning on Monday about an increased risk of an autoimmune disorder, Guillain-Barre, linked to the Johnson & Johnson COVID vaccine.
The United States Food & Drug Administration or the FDA issued an announcement that Dole Diversified North America, Inc. has recalled a specified number of cases of its fresh blueberries because of a possible cyclospora contamination.
Former Food and Drug Administration (FDA) commissioner Scott Gottlieb said the Delta variant is likely to become the dominant COVID strain in the United States.
Three members of an independent panel that advised the U.S. FDA on nervous system drugs had resigned after the agency approved an Alzheimer's drug from Biogen.
Another COVID-19 antibody-drug has been given emergency use approval by the U.S. Food and Drug Administration. The said drug was developed by GlaxoSmithKline and Vir Biotechnology.
Based on the Food and Drug Administration, the studies suggest that the ban on menthol would help individuals to quit smoking. The FDA noted that menthol makes tobacco more palatable and the flavor facilitates progression to regular smoking, especially to youth and young adults.
An advisory panel to the U.S. Food and Drug Administration (FDA) voted unanimously on Friday to recommend that the agency approve the use of Johnson & Johnson's COVID-19 vaccine in adults.
A New York health care worker suffered from a severe allergic reaction after receiving the first shot of a coronavirus vaccine, city officials said on Wednesday.
