HHS Secretary RFK Jr. orders FDA to close food ingredients loophole
Health and Human Services Secretary Robert F. Kennedy Jr. ordered the Food and Drug Administration on Monday to revise its ...
News Medical on MSN2d
How the FDA Opens the Door to Risky Chemicals in America's Food Supply
In 1958, Congress mandated that, before additives could be used in foods, manufacturers had to prove they were safe and get ...
How the FDA lets chemicals pour into America's food supply
Chemicals such as titanium dioxide and potassium bromate, whose safety has been debated, are allowed in foods in the United ...
Trump’s pick to lead FDA tells senators he’d look into food, abortion pill, vaccine advisers
President Donald Trump’s pick to lead the US Food and Drug Administration told senators in a tense confirmation hearing ...
A Spending Freeze at the FDA Threatens Safety of Food Supply, Current Staffers Say
FDA staffers tell CR how the suspension of their discretionary spending is threatening the safety of the American food supply ...
Girl Scouts hit with lawsuit over alleged heavy metals, toxins in its cookies
Last month, a non-peer-reviewed study commissioned by Moms Across America alleged that Girl Scout Cookies had toxins in them.
Tasting Table on MSN1d
The Difference Between FDA And USDA Food Regulations, Explained
We've all seen the various inspection labels at the grocery store and heard news about food recalls. But what's the actual ...
USDA Disbands Two Key Food Safety Committees
WEDNESDAY, March 12, 2025 (HealthDay News) -- Two key federal advisory committees on food safety have been shut down, raising ...
Girl Scouts lawsuit makes claims about metals, toxins in cookies. 5 things to know
The class action against the Girl Scouts of America and manufacturers Ferrero U.S.A. and ABC Bakers was filed on Monday, ...
Kennedy gives food company CEOs an ultimatum
Robert F. Kennedy Jr. delivered a stark ultimatum to major food company CEOs in a closed-door meeting this week: Ban certain ...
EurekAlert!1d
Over 1.2 million medical device side-effect reports not submitted within legal timeframe
Over 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) within the deadline set by federal regulations, finds an analysis of recent data ...