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FDA rehires staff to its medical devices division

FDA moves to rehire medical device, food safety and other staffers fired 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,

Yahoo · 17h

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,

Penn Live · 22h

FDA rehires medical device staffers fired only days earlier

Like other agencies, the FDA terminations went to employees in their probationary period, typically the first two years of federal employment. But that approach resulted in the te

Drug compounders sue FDA over semaglutide status

BioPharma Dive · 41m

Drug compounders sue FDA over declaration ending Wegovy shortage

Telehealth provider Hims & Hers said it will tell consumers they need to seek “alternative options on the commercial dosing,” but in earnings Monday still forecast higher revenue and profits in 2025.

FiercePharma · 3h

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.

BioSpace · 4h

Compounders Sue FDA for Declaring Ozempic, Wegovy Shortage Over

The Outsourcing Facilities Association, a trade group representing compounders, filed a similar lawsuit in October last year after the FDA formally ended the tirzepaptide shortage.

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 · 20h

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 · 23h

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.

Business Insider · 1d

Pfizer names Patrizia Cavazzoni Chief Medical Officer

Pfizer (PFE) announced that Patrizia Cavazzoni will rejoin the company as Chief Medical Officer. Cavazzoni was most recently Director of the

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 · 7h

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.

58mon 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 ...

17hon 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 ...

STAT2h

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 ...

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, ...

19h

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 ...

1don 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, ...

FierceBiotech5h

FDA updates Boston Scientific’s Accolade pacemaker recall, reporting 832 injuries

The FDA is further elevating a pacemaker recall from Boston Scientific that it first broadcasted in December, over certain ...

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 ...

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FDA rehires staff to its medical devices division

Drug compounders sue FDA over semaglutide status

FDA, recall and Nationwide

Pfizer names former FDA director

Medtronic gets FDA approval for Brainsense device

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