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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 · 7h

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 · 12h

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

Listeria, FDA

CNN · 9h

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,

Fox Business · 1d

Frozen shakes served at nursing homes recalled after being linked to numerous deaths, hospitalizations: FDA

The FDA announced that a food distributor is recalling all ReadyCare and Sysco Imperial Frozen Supplemental shakes, typically sold to long-term care facilities, over listeria concerns.

U.S. News & World Report · 11h

US FDA, CDC Investigating Multi-State Listeria Outbreak

The U.S. FDA 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.

FDA, Snack and recall

Newsweek on MSN · 16h

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 · 14h

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 · 10h

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 hires ex-FDA drug chief

Reuters · 16h

Pfizer names former FDA director Patrizia Cavazzoni as chief medical officer

Pfizer said on Monday former head of FDA's drug center, Patrizia Cavazzoni, will join the drugmaker as chief medical officer.

STAT · 14h

Patrizia Cavazzoni, former head of FDA’s drug center, joins Pfizer as chief medical officer

Patrizia Cavazzoni, formerly the top regulator of the drug division of the FDA, will join Pfizer as chief medical officer.

The Hill on MSN · 12h

Pfizer hires ex-FDA drug chief as top doctor

The former head of the Food and Drug Administration’s (FDA) drug division is joining Pfizer as its chief medical officer, the company announced Monday. Patrizia Cavazzoni was formerly director of

Medtronic, Parkinson's disease and FDA

Reuters · 18h

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 · 18h

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.

Minneapolis Star Tribune on MSN · 6h

In Parkinson’s fight, Medtronic’s first-in-the-world adaptive therapy feature wins FDA approval

After decades of development and trials, Medtronic has secured U.S. Food and Drug Administration approval for adaptive technology personalizing treatment of Parkinson’s symptoms using advanced stimulation deep in the brain.

6hon 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 to meet before they can be labeled as “healthy” on their ...

FierceBiotech16h

FDA works to reverse layoffs, rehire lost staff: reports

After hundreds of FDA employees were suddenly laid off last weekend, including dozens at the agency’s device center, 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, ...

17h

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 ...

16h

Ice Cream Recall Elevated To FDA’s Deadliest Category—But There’s A Catch

Seeing the words "Class I food recall" might make you think of contaminated products sitting on grocery store shelves, but ...

9hon MSN

FDA and USDA among federal agencies aiming to rehire workers hit by mass firings

A number of agencies are looking to rehire federal workers who lost their jobs as part of the Trump administration's mission ...

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

The lawsuit claims the FDA's finding that there was no longer a shortage of the drugs' active ingredient semaglutide was ...

13h

Yearslong shortage of popular weight-loss and diabetes drugs resolved, FDA says

Shortages of Ozempic and Wegovy that have been in place for more than two years have been resolved, as supplies of obesity ...

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FDA rehires staff to its medical devices division

Listeria, FDA

FDA, Snack and recall

Pfizer hires ex-FDA drug chief

Medtronic, Parkinson's disease and FDA

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