While it caused cancer in these male rats, the dye does not cause cancer in humans and other animals in the same way, according to other studies. Therefore, “claims that the use of FD&C Red No. 3 in food and in ingested drugs puts people at risk are not supported by the available scientific information,” according to the FDA.

Federal health authorities have upgraded their recall of 13-ounce bags of Frito-Lay potato chips over fears that consuming the products, which may contain undeclared milk, could potentially be fatal. Last month, the Food and Drug Administration announced that Frito-Lay was voluntarily recalling a limited batch of products.

A recall which was issued across nine states has now been given the highest risk classification by the federal agency.

Aaron Siri, a lawyer advising Robert F. Kennedy Jr. as he prepared to become health secretary, petitioned the Food and Drug Administration in 2022 to revoke approval of a polio vaccine that is used widely in the U.

A New York aesthetician was arrested on Wednesday for allegedly buying counterfeit Botox from China and injecting it into patients, prosecutors said.

The petition, first reported by the New York Times, asked the Food and Drug Administration ... It came five months after then-President Donald Trump proudly announced the FDA's green light of the vaccine was imminent. "They say it's somewhat of a miracle ...

Those with an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume the recalled product,” the FDA said in its initial notice on Dec. 16.

A corn puff recall has been expanded to include two more products over concerns the snacks could cause “serious or life-threatening” allergic reactions, federal officials said. The recall of Shirakiku Curvee Puffs Corn Puff Snack now includes its Sea Salt & Umami Flavor and its Corn Potage Flavor for undeclared milk, according to the FDA.

From medical devices to OTC drugs, preemption to expert preclusion, New York state and federal courts issued decisions in 2024 which further

The Food and Drug Administration has updated the recall of Broccoli florets sold at Walmart to class I risk level, which is the highest level of risk.

It’s the first new pharmaceutical approach to treating pain in more than 20 years, offering an alternative to both opioids and over-the-counter medications.

( The Hill) – The U.S. Food and Drug Administration (FDA) approved Journavx (suzetrigine) oral tablets on Thursday as a first-in-class non-opioid analgesic to treat acute pain in adults.