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FDA, deodorant

FDA Issues Highest Risk Warning For Mushroom Recall

Mushrooms sold across two states have been recalled over fears they could be harboring listeria, a bug that "can cause serious and sometimes fatal infections."

AL.com on MSN · 6h

FDA deodorant recall is nationwide: What should you do if you own one of the products?

The Food and Drug Administration has recalled more than 67,000 cases of deodorant sold at major retailers due to manufacturing practices that violate federal regulations.

TODAY on MSN · 9h

The FDA just recalled 67,000 cases of deodorant — here’s what you need to know

But one thing we’re confident about is that nobody wants to use a deodorant that has been recalled, which is why we are sharing this news: The Food and Drug Administration has issued a recall on 67,000 cases of Power Stick antiperspirant deodorant.

FDA Appoints Biotech Executive as Top Drug Regulator

Associated Press News on MSN · 12h

FDA names former pharmaceutical company executive to oversee US drug program

The Food and Drug Administration named a longtime pharmaceutical executive to run the agency’s drug program. Dr.

Bloomberg on MSN · 12h

FDA appoints biotech executive as top drug regulator under RFK Jr.

Food and Drug Administration commissioner Marty Makary has chosen former biotech executive George Tidmarsh as the agency’s top drug regulator, the agency confirmed Monday.

UPI on MSN · 10h

Biotech exec George Tidmarsh picked as FDA's chief drug regulator

The U.S. Food and Drug Administration named ex-biotech exec George Tidmarsh as its chief drug regulator. FDA Commissioner Marty Makary called Tidmarsh an "accomplished physician-scientist and leader."

FDA Shuts Down Sarepta Gene Therapy Trials

Newsweek on MSN · 1d

FDA Suspends Muscular Dystrophy Drug After 3 Patient Deaths

The U.S. Food and Drug Administration ( FDA) has placed an immediate clinical hold on Sarepta Therapeutics' investigational gene therapy trials for limb girdle muscular dystrophy following three patient deaths potentially linked to the company's treatments.

MarketWatch · 15h

FDA Places Sarepta's Investigational Gene-Therapy Trials on Hold Following Patient Death

The Food and Drug Administration placed a clinical hold on Sarepta Therapeutics' investigational gene-therapy clinical trials for limb-girdle muscular dystrophy, a group of genetic disorders that cause muscles to weaken and atrophy.

MyChesCo on MSN · 10h

FDA Shuts Down Sarepta Gene Therapy Trials After Three Deaths Linked to Liver Failure

The U.S. Food and Drug Administration on Friday placed Sarepta Therapeutics’ gene therapy trials for limb girdle muscular dystrophy on clinical hold following the deaths of three patients

STAT8h

New head of FDA drug center is a biotech veteran and an outspoken critic of the academic establishment

The Food and Drug Administration on Monday named George Tidmarsh, a longtime biotech executive who has a background in ...

FDA Announces Major Recall of Popular Chocolate Item

It's a good thing the U.S. Food and Drug Administration is staying on top of the latest recalls, because knowing about new ...

FDA Approves Prefilled Syringe Presentation for Shingles Vaccine

Prefilled syringe eliminates the need to reconstitute separate vials prior to administration and simplifies the vaccine ...

FDA panel promotes misinformation about antidepressants during pregnancy

NBC News medical contributor Dr. Natalie Azar reports on the FDA panel discussion of the use of antidepressants during ...

16hon MSN

FDA Greenlights Game-Changing UV Technology That Could Make Raw Milk Safer to Consume

Tamarack Biotics’ TruActive process targets pathogens with UV light while keeping the milk’s enzymes and proteins intact.

14h

FDA Elevates Dubai Chocolate Spread Recall to Class 1 Over Salmonella Risk

Salmonella can cause serious and potentially fatal infections in young children, the frail or elderly, and others with ...

Las Vegas Sun1d

Juul’s FDA approval doesn’t clear fog of e-cigarette risks, especially for teens

The Food and Drug Administration has granted permission for Juul to continue selling its e-cigarettes, offering some reprieve ...

Targeted Oncology16h

FDA Issues Complete Response Letter for Glofitamab in R/R DLBCL Combination Therapy

FDA issues a complete response letter for glofitamab's second-line DLBCL indication, highlighting ongoing scrutiny in ...

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FDA, deodorant

FDA Appoints Biotech Executive as Top Drug Regulator

FDA Shuts Down Sarepta Gene Therapy Trials

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