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FDA rehires staff to its medical devices division

Hosted on MSN · 2h

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 · 23h

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,

U.S. News & World Report · 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medical devices and other key areas received calls and emails notifying them that their recent terminations had been “rescinded effective immediately,

Listeria, FDA and Shakes Kills 12

CNN · 23h

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,

Reuters · 23h

US FDA, CDC investigating multi-state listeria outbreak

The U.S. Food and Drug Administration and the Centers for Disease Control and Prevention said on Monday the agencies were investigating a multi-state outbreak of listeria infections linked to frozen supplemental shakes manufactured by Prairie Farms Dairy Inc.

U.S. News & World Report · 5h

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

The Hill · 1h

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

FiercePharma · 6h

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.

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 · 1d

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.

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

STAT6h

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 ...

4hon 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 ...

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, ...

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 ...

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, ...

Targeted Oncology1h

FDA Grants Perioperative Pembrolizumab Priority Review in HNSCC

The FDA granted priority review to pembrolizumab for neoadjuvant and adjuvant use in head and neck squamous cell carcinoma, ...

Healio1h

FDA approves first adaptive deep brain stimulation system for Parkinson’s disease

The FDA has approved BrainSense, an adaptive deep brain stimulation system that can adjust therapy for Parkinson’s disease in real time based on the patient’s brain activity, according to the ...

2hon MSN

Fury as Trump's drug chief quits to join Pfizer for mega salary

Health experts have slammed the FDA as 'corrupt' and 'in bed with Big Pharma' after its former drug chief Dr Patrizia ...

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FDA rehires staff to its medical devices division

Listeria, FDA and Shakes Kills 12

Drug compounders sue FDA over semaglutide status

FDA, recall and Nationwide

Pfizer names former FDA director

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