Peanut butter recall update for 40 states as FDA sets risk level

It means the products may cause temporary or medically reversible adverse health consequences, according to the FDA.
Fierce Biotech

FDA rejects Disc’s rare disease drug despite commissioner’s voucher

The FDA has rejected a rare blood disease candidate from Disc Medicine, a compound that been granted expedited review through a newly launched priority voucher program.

US FDA declines to approve Disc Medicine's rare disease drug

Feb 13 (Reuters) - Disc Medicine said on Friday the U.S. Food and Drug Administration has declined to approve its drug to treat a rare genetic disorder, sending its shares down more than 20% by the close.

Cake Mix Recall Update as FDA Sets Most Serious Risk Level

This classification is used when the FDA finds a reasonable chance that exposure could cause serious harm or death.

FDA Reviews Safety of Food Preservative BHA Over Cancer Concerns

“BHA has remained in the food supply for decades despite being identified by the National Toxicology Program as ‘reasonably anticipated to be a human carcinogen’ based on animal studies,” U.S. Department of Health and Human Services Secretary Robert F. Kennedy Jr ., said.

FDA moves to ban BHA — an additive used in processed foods such as meats and bread

The Food and Drug Administration on Tuesday took steps toward banning BHA, a food additive used in processed foods such as meats and bread

Tom Cotton demands FDA probe into illegal Chinese ingredients in US weight loss drugs

Ark., warned that up to 1.5 million Americans may be using weight loss medications with potentially dangerous Chinese ingredients.

Moderna blames FDA for threatening US leadership in medicine

Moderna Inc. lashed out at the US Food and Drug Administration for making it harder for companies to create new medicines, escalating a dispute between the vaccine maker and the regulator.