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Listeria, FDA and Shakes Kills 12

Map Shows States With Listeria Cases as FDA Recalls Nutritional Shake

A nationwide recall of frozen nutritional shakes has been issued after a listeria outbreak tied to the drinks resulted in multiple hospitalizations and deaths across the United States, according to the U.

CNN · 1d

Listeria outbreak linked with supplemental shakes now stands at 12 deaths, FDA says

Twelve deaths have been reported as part of an outbreak of Listeria monocytogenes infections linked to frozen supplemental shakes, the US Food and Drug Administration said Monday. At least 38 people in 21 states had been infected,

U.S. News & World Report · 1d

Listeria Outbreak From Frozen Shakes Kills 12, Sickens 38

A listeria outbreak tied to frozen shakes served in hospitals and long-term care facilities has sickened at least 38 people and killed 12, according to the U.S. Food and Drug Administration (FDA). The shakes,

Drug compounders sue FDA over semaglutide status

Reuters · 1d

Drug compounders sue US FDA over removal of Wegovy, Ozempic from shortage list

Drug compounders sued the U.S. Food and Drug Administration on Monday over its decision last week to remove Novo Nordisk's weight-loss and diabetes treatments Wegovy and Ozempic from its shortage list,

The Hill on MSN · 19h

Drug compounders sue over weight loss drugs’ removal from FDA shortage list

A trade group representing compounding pharmacies has filed a lawsuit against the Food and Drug Administration (FDA) for removing semaglutide, the active ingredient in Ozempic, from its drug

The National Law Review · 21h

GLP-1 Drugs: FDA Removes Semaglutide from the Drug Shortage List

On February 21, 2025, the U.S. Food and Drug Administration (FDA) issued a Declaratory Order determining that the semaglutide drug shortage has been resolved. The timing of this order was unexpected due to the ongoing litigation between FDA and the Outsourcing Facilities Association (OFA) involving tirzepatide,

Trump Accidentally Fired FDA Medical Device Reviewers

HuffPost on MSN · 21h

Oops! Trump Accidentally Fired FDA Medical Device Reviewers

The Food and Drug Administration is scrambling to bring back hundreds of critical workers laid off en masse by DOGE.

NBC News on MSN · 1d

FDA rehires staff to its medical devices division after mass layoffs

The Trump administration is reinstating some employees in the Food and Drug Administration's medical devices division after dozens were laid off as part of a government-wide cost-cutting initiative led by billionaire Elon Musk and his Department of Government Efficiency,

ABC · 1d

FDA moves to rehire medical device staffers fired only days earlier

Barely a week after mass firings at the Food and Drug Administration, some probationary staffers received unexpected news over the weekend: The government wants them back. Beginning Friday night, FDA employees overseeing medical devices and other key areas received calls and emails notifying them that their recent terminations had been “rescinded effective immediately,

1don MSN

FDA delays when a final rule on what foods can be labeled as ‘healthy’ goes into effect

The US Food and Drug Administration’s new standards for foods before they can be labeled as “healthy” on their packaging will ...

STAT18h

Trump’s FDA navigates layoffs, exits, and a new hire

The Trump administration has started rehiring some of the FDA employees it fired last week, the latest chapter in a haphazard ...

15h

'This guy': Trump Jr.’s hunting buddy to be top food regulator at FDA

What we are seeing from this administration is literally an inversion of a merit-based system—a spoils system for cronies and ...

Ex-FDA commissioner on implications of agency’s ‘unreasonable’ jobs cuts

Dr. Robert Califf, former FDA commissioner and instructor at Duke Department of Medicine, explains the negative implications ...

2don MSN

FDA Asks 300 Fired Scientists to Return

The FDA plans to rehire around 300 people in total, according to four sources with secondhand knowledge of the situation, ...

FiercePharma2h

FDA dings Piramal API plant with Form 483 detailing problems tied to quality control, equipment cleaning and more

Roughly a year after receiving an FDA reprimand at its manufacturing plant in Michigan, Indian drugmaker Piramal Pharma has ...

23hon MSN

Smokescreen: some vape firms pivot after FDA crackdown

Such tactics have complicated U.S. efforts to stem the flow of vapes lacking authorisation into the country, according to the ...

49mon MSN

Baby Food Recalled in 45 States as FDA Sets Highest Risk Level

The U.S. Food and Drug Administration (FDA) has given its most serious risk level, Class I, to teething stick products from Gerber Products Company due to a choking hazard. According to the FDA, a ...

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Listeria, FDA and Shakes Kills 12

Drug compounders sue FDA over semaglutide status

Trump Accidentally Fired FDA Medical Device Reviewers

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