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FDA recalls over 67,000 cases of Power Stick 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."

TODAY on MSN · 13h

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.

Austin American-Statesman on … · 20h

FDA recalls over 67,000 cases of Power Stick deodorant due to manufacturing violations

What deodorant products are being recalled? Where were the recalled products sold? According to the recall notice, the Power Stick deodorants were sold nationwide. The deodorants

FDA Appoints Biotech Exec

USA TODAY · 15h

FDA appoints biotech veteran George Tidmarsh to lead drug evaluation division

Stanford's George Tidmarsh has authored 143 scientific papers and patents, as well as played a central role in developing seven FDA-approved drugs.

Bloomberg on MSN · 17h

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 · 15h

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

MyChesCo on MSN · 15h

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

MarketWatch · 20h

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.

InvestorsHub on MSN · 18h

Sarepta Shares Drop as FDA Suspends Gene Therapy Trials for Muscular Dystrophy

Shares of Sarepta Therapeutics Inc (NASDAQ:SRPT) plunged 10% after the company disclosed that the U.S. Food and Drug Administration (FDA) has imposed a clinical hold on several of its gene therapy programs targeting limb girdle muscular dystrophy (LGMD).

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 ...

STAT12h

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 ...

12h

FDA Approves Prefilled Syringe Presentation for Shingles Vaccine

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

BioSpace18h

FDA’s CDER Gets New Chief in Biopharma Veteran George Tidmarsh

Tidmarsh, an adjunct professor at Stanford’s medical school, brings decades of industry experience to the table. Serving as ...

9hon MSN

FDA panel promotes misinformation on antidepressants during pregnancy, psychiatrists say

A Food and Drug Administration panel on Monday discussing the use of antidepressants during pregnancy largely amounted to ...

18h

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 ...

20hon 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.

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 ...

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