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FDA Will Ask Sarepta to Halt Gene Therapy Shipments

Exclusive: Sarepta says it won't comply with FDA request to stop shipping gene therapy Elevidys

U.S. regulators asked Sarepta Therapeutics on Friday to voluntarily halt shipments of its Elevidys gene therapy after a muscular dystrophy patient who received a different, experimental treatment died,

Associated Press News on MSN · 9h

Gene therapy maker Sarepta tells FDA it won't halt shipments despite patient deaths

Drugmaker Sarepta Therapeutics said late Friday it won't comply with a request from the Food and Drug Administration to halt all shipments of its gene therapy following the death of a third patient receiving one of its treatments for muscular dystrophy.

The Boston Globe · 1d

FDA prepares to ask Sarepta Therapeutics to stop all shipments of Duchenne muscular dystrophy therapy

The move follows the death of two teenagers who were administered the treatment, as well as the death of a 51-year-old man who received a similar product in a clinical trial for a different form of muscular dystrophy.

FDA, Recall and Deodorant

Yahoo · 4h

FDA Announces Major Recall of Popular Deodorant

It's important to stay informed about recalls, because doing so truly impacts your life. Of course, the sooner you know about a recall, the better, because you can make sure to get rid of the suspecting item and keep everyone in your family safe.

Austin American-Statesman on M… · 1d

FDA recalls over 67,000 cases of Power Stick deodorant. See where products were sold

The manufacturer announced a recall of 67,214 cases of its Power Stick roll-on deodorant due to violations of Current Good Manufacturing Practices.

al.com · 1d

Deodorant recall: More than 67,000 cases sold at Walmart, Dollar Tree, Amazon

More than 67,000 cases of deodorant sold at major retailers are being recalled due to a manufacturing issue. According to a notice from the FDA, Pennsylvania-based cosmetics brand A.P. Deauville has launched a recall for over 67,

FDA Approves JUUL E-Cigs for Sale

Politico · 1d

FDA makes Juul’s reign official

JUUL GETS ITS CROWN — The FDA authorized Juul’s applications on Thursday to sell e-cigarettes in the U.S., determining they’re “appropriate for the protection of public health” because their benefits to adult smokers of combustible cigarettes outweigh the risks to nonsmoking youths.

UPI on MSN · 2d

FDA approves Juul e-cigarette and cartridge sales

Officials with the Food and Drug Administration have approved the continued sales of tobacco-flavored e-cigarettes and refill cartridges by Juul Labs.

U.S. News & World Report · 1d

FDA Approves Juul E-Cigs for Sale, Years After Ban Attempt

The U.S. Food and Drug Administration (FDA) said that it will allow Juul to market its e-cigarette device and tobacco and menthol refill cartridges. The agency said the products may help adult smokers quit traditional cigarettes.

1don MSN

FDA Issues Risk Warning for Ice Cream Recalled in 23 States

Rich Ice Cream Co. recalled numerous lots of its products on June 27 over potential contamination with Listeria monocytogenes ...

FDA Plans to Revoke 52 Food Standards

The 52 food standards pertain to canned fruits and vegetables, dairy products, baked goods, macaroni products, and other ...

1don MSN

FDA Authorizes Juul’s E-Cigarettes After Ban Nearly Bankrupted Firm

The regulator authorized the company to keep its e-cigarettes on the U.S. market after a federal ban in 2022 had pushed it to ...

3don MSN

FDA to end dozens of 'obsolete' rules for U.S. food items

The U.S. government is nixing a whole slew of "obsolete" U.S. food standards that Trump administration officials say also ...

MedPage Today on MSN15h

FDA Advisors Give PTSD Drug Combination a Thumbs Down

"I may have been swayed if this represented a major advance in the field," said panelist Walter Dunn, MD, PhD, of the ...

The FDA's Newest Approval Could Have A Major Impact On Your Favorite Foods

Move over, artificial food colors, the FDA just approved gardenia (genipin) blue, a plant‑derived dye to shake up drinks and ...

FDA panel reassesses hormone therapy warnings in menopause treatments

The Food and Drug Administration is reassessing some warnings given about hormone therapy treatments for menopause that have ...

1don MSN

FDA recalls frozen sprouted beans produced by Sugarland company for links to salmonella outbreak

Health officials have recalled two products produced by Chenak LLC, which has a location in Sugarland, for ties to a ...

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FDA Will Ask Sarepta to Halt Gene Therapy Shipments

FDA, Recall and Deodorant

FDA Approves JUUL E-Cigs for Sale

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