There are Americans who are "obscenely obese and at the same time malnourished," Health and Human Services Secretary Robert F ...
This classification is used when the FDA finds a reasonable chance that exposure could cause serious harm or death.
The Food and Drug Administration rejected Moderna's new flu shot. This raises questions about what it means for the future of vaccine development.
The FDA upgraded a nationwide cake mix recall to Class I due to undeclared milk allergens, posing serious health risks for ...
Vibroacoustic Products Listed as Class I Medical Devices; Red Light Therapy Products Listed as Class II Medical Devices ...
The flu vaccine is its first using mRNA technology for influenza.
Richard Pazdur, a longtime regulator, said politics risks outweighing science at the agency.
The FDA has rejected a rare blood disease candidate from Disc Medicine, a compound that been granted expedited review through ...
The Food and Drug Administration on Tuesday took steps toward banning BHA, a food additive used in processed foods such as ...
By Mariam Sunny and Michael Erman Feb 13 (Reuters) - Moderna said it is looking for growth overseas after the U.S. FDA refused to review its experimental flu shot and the country's top health ...
PHOENIX, AZ - February 02, 2026 - PRESSADVANTAGE - Phoenix NP, a women-focused telehealth medical practice based in ...
It means the products may cause temporary or medically reversible adverse health consequences, according to the FDA.