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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 · 12h

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 … · 19h

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 Executive as Top Drug Regulator

USA TODAY · 14h

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 · 16h

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.

Associated Press News on MSN · 17h

FDA names former pharmaceutical company executive to oversee US drug program

The Food and Drug Administration on Monday named a longtime pharmaceutical executive to run the agency’s drug program, the latest in a string of leadership changes at the agency. FDA Commissioner Marty Makary announced that Dr.

FDA suspends muscular dystrophy drug

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.

MedPage Today · 14h

Drugmaker Refuses FDA's Request to Pull Gene Therapy Tied to Patient Deaths

The agency also revoked Sarepta's platform technology designation for AAVrh74 Friday and issued a safety communication saying the agency was investigating the three deaths due to acute liver failure following treatment with Sarepta's AAVrh74 gene therapies.

InvestorsHub on MSN · 17h

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).

STAT11h

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 ...

11h

FDA Approves Prefilled Syringe Presentation for Shingles Vaccine

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

20hon MSN

FDA to appoint George Tidmarsh as top drug regulator, Bloomberg News reports

U.S. Food and Drug Administration commissioner Marty Makary has chosen former biotech executive George Tidmarsh as the ...

8hon 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 ...

8hon MSN

FDA Announces Massive Ice Cream Recall in 23 States

The Food and Drug Administration (FDA) makes sure to stay on top and notify people whenever a recall is put into place.

17h

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 ...

19hon 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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News

FDA recalls over 67,000 cases of Power Stick deodorant

FDA Appoints Biotech Executive as Top Drug Regulator

FDA suspends muscular dystrophy drug

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