Neuralink announced that it has received the U.S. Food and Drug Administration's (FDA) "breakthrough" tag to restore communication for those with severe speech impairment.
The Illinois House of Representatives, led by Democrats, has passed House Bill 3637, aiming to ensure continued access to abortion medication, specifically mifepristone, regardless of potential federal restrictions.
The U.S. Food and Drug Administration (FDA) has announced a recall of multiple over-the-counter acne treatments due to the presence of benzene, a chemical linked to cancer. Retailers have been instructed to remove the affected products from shelves and online marketplaces.
The Food and Drug Administration (FDA) has announced a recall of nearly 2,800 containers of First Aid Beauty’s Ultra Repair Cream in Coconut Vanilla due to a “Current Good Manufacturing Practice deviation.”
An Indiana family is demanding accountability from the U.S. Food and Drug Administration (FDA) after their 9-year-old son, Colton George, nearly died from a severe E. coli infection that caused his kidneys to fail.
On January 16, 2025, U.S. District Judge Matthew Kacsmaryk in Amarillo, Texas, ruled that Idaho, Missouri, and Kansas can continue their lawsuit against the U.S. Food and Drug Administration (FDA) seeking to restrict the availability of the abortion pill mifepristone.
In the final days of President Joe Biden’s administration, federal officials unveiled a proposal to reduce nicotine levels in cigarettes, a move aimed at curbing addiction and reducing smoking rates. The Food and Drug Administration (FDA) has been working on this initiative for years, marking a significant step in tobacco regulation.
The Food and Drug Administration (FDA) announced that it will ban Red No. 3 in food, drinks, and pharmaceutical products. Red No. 3 is a synthetic coloring frequently used in candies, desserts, and some drugs.
