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The nacho cheese chips contain undeclared milk, which could cause a serious or life-threatening allergic reaction to those with an allergy or severe sensitivity to milk, the FDA said in a press ...
Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. visited employees at the FDA on Friday and reportedly told them that "the Deep State is real." The visit was his first appearance ...
The Food and Drug Administration (FDA) has warned men against taking an “adulterated” dietary supplement that boosts libido after it was found to contain sildenafil citrate—the same drug ...
NBC News obtained a recording of Kennedy’s address, his first joint appearance with the new FDA commissioner, Dr. Marty Makary. The event was meant to welcome both men and highlight the agency ...
To get FDA approval, scientists must be able to demonstrate that a new drug or treatment is safe and effective. And currently, before they can test a new therapy in humans, they must show proof ...
According to the FDA, the recall was initiated March 26. The 189 cases of butter were sold in stores in Vermont, New York, Pennsylvania, Maine, Connecticut, New Hampshire, and Arkansas.
The Food and Drug Administration (FDA) announced it has elevated a recall it issued last month for one of its most popular chip brands due to an undeclared allergen. Frito-Lay initially issued the ...
Layoffs at the Food and Drug Administration are expected to reduce the FDA's workforce by 20%. Susan Mayne, former director of the Center for Food Safety and Applied Nutrition at the FDA ...
Minnesota is home to hundreds of medical device companies that can't sell new technologies or produce revenue without FDA review. A federal official did not answer questions about the cause of the ...
U.S. Food and Drug Administration approvals of life-changing, high-risk medical devices reportedly slowed to a 10-year low for the January to March period, as recent layoffs have reportedly had ...
A "first of its kind" surgery developed in Minnesota to provide relief from debilitating back pain is one step closer to FDA approval. WCCO first learned about SynerFuse in 2023 after a patient ...
On March 26, 2025, the Company announced that the U.S. Food and Drug Administration (FDA) issued an Approvable Letter regarding the Company's Pre-Market Approval (PMA) application for the Genio ...
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