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FDA wants fired medical device staffers back at work

HuffPost on MSN · 1h

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.

The Associated Press on MSN · 1d

FDA Moves to Rehire Medical Device Staffers Fired Only Days Earlier

The reversal is the latest example of President Donald Trump and billionaire Elon Musk's chaotic approach to cost-cutting, which has resulted in several agencies firing, and then scrambling to rehire, employees responsible for nuclear weapons, national parks and other government services.

Yahoo · 20h

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,

FDA, Semaglutide

FiercePharma · 5h

Compounders sue FDA again over declaring end of shortage for Novo's semaglutide

Compounding pharmacies aren’t surrendering their ability to create cheaper knockoff versions of Eli Lilly and Novo Nordisk’s weight loss drugs without a fight. | Compounding pharmacies aren’t surrendering their ability to create cheaper knockoff versions of Eli Lilly and Novo Nordisk’s weight loss drugs without a fight.

CBS News on MSN · 2d

FDA declares end to Wegovy and Ozempic shortage

The agency first declared a shortage of semaglutide, the main ingredient used to make Ozempic and Wegovy, in 2022.

The National Law Review · 1h

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,

FDA, recall and Nationwide

Newsweek on MSN · 1d

Nationwide Mac & Cheese Snack Recall As FDA Issues Risk Warning

Feel Good Foods Inc. issued a voluntary recall for thousands of cases of its Mac & Cheese Bites in February due to the possible presence of metal pieces.

AL.com on MSN · 1d

Nationwide recall issued for popular snack food as FDA sets risk warning

A batch of recalled frozen mac and cheese bites have been issued a Class II risk classification by the U.S. Food and Drug Administration (FDA). Newsweek reports Feel Good Foods Inc. has issued a voluntary recall for its Three Cheese Mac & Cheese Bites due to the possible presence of metal pieces.

Allrecipes on MSN · 23h

FDA Announces Nationwide Recall of Frozen Snack Due to Possible Metal Contamination

The recall was initially issued on Feb. 5 by Feel Good Foods, though the FDA recently updated it to a Class II event. A Class II recall (which is the second-most severe risk level) indicates "a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Pfizer names former FDA director

Reuters · 1d

Pfizer names former FDA director as chief medical officer

Pfizer on Monday named the former head of the U.S. health regulator's drug evaluation unit, Patrizia Cavazzoni, as its chief medical officer, bringing back an industry veteran to lead its regulatory and drug safety operations.

Bloomberg on MSN · 1d

Pfizer Names Former FDA Drug Chief as Top Doctor

Pfizer Inc. appointed the Food and Drug Administration’s former top drug reviewer to serve as its chief medical officer.

Seeking Alpha on MSN · 1d

Pfizer taps former FDA drug chief as chief medical officer

Pfizer (NYSE:PFE) has tapped Patrizia Cavazzoni, the former head of drug regulation at the FDA, as its new chief medical officer. Cavazzoni was most recently director of the Center for Drug Evaluation and Research (CDER) at the U.

Medtronic gets FDA approval for Brainsense device

Reuters · 1d

US FDA approves Medtronic's medical device for Parkinson's disease

The U.S. Food and Drug Administration has approved Medtronic's deep brain stimulation system for use in patients with Parkinson's disease, the medical device maker said on Monday.

MarketWatch · 1d

Medtronic Parkinson's Disease Brain Stimulation System Gets FDA Approval

Medtronic said the Food and Drug Administration approved a brain stimulation system for people afflicted with Parkinson's disease. The medical technology company said the regulator approved BrainSense Adaptive deep brain stimulation and BrainSense Electrode Identifier.

Axios Vitals on MSN · 9h

FDA OKs adaptive brain pacemaker for Parkinson's treatment

The Food and Drug Administration on Monday granted its first approval for a pacemaker-like device for the brain to ease symptoms of Parkinson's disease, which affects nearly 1 million people in the United States.

7hon MSN

Smokescreen: some vape firms pivot after FDA crackdown

Some e-cigarette companies targeted by U.S. authorities have altered their business model or changed their corporate ...

STAT5h

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 ...

22h

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 ...

US FDA asks fired scientists to return, including some reviewing Musk’s Neuralink

The U.S. Food and Drug Administration is asking some of its recently fired scientists if they will come back to their jobs, ...

22h

Trump Administration Reverses Layoffs At These Federal Agencies—After Cutting Bird Flu, FDA Staff

Some employees at the National Nuclear Security Administration, which oversees the U.S.’ nuclear weapons, were reportedly ...

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 ...

How the FDA's approval for food additives works, and why experts say a loophole allows companies to bypass it

Experts say that for decades, a legal loophole has allowed companies to include chemical additives that could be potentially ...

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FDA wants fired medical device staffers back at work

FDA, Semaglutide

FDA, recall and Nationwide

Pfizer names former FDA director

Medtronic gets FDA approval for Brainsense device

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