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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

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 · 2h

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 · 6h

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 · 4h

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,

Hosted on MSN · 5h

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.

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.

Drug compounders sue FDA over semaglutide status

Reuters · 6h

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

Drug compounders on Monday sued the U.S. Food and Drug Administration over its decision last week to remove Novo Nordisk's weight loss and diabetes drugs Wegovy and Ozempic from its shortage list, a move that will sharply curtail the compounders' ability to sell cheaper versions of the drugs.

Seeking Alpha on MSN · 2h

Drug compounders sue FDA over semaglutide status: report

Makers of copycat versions of Novo Nordisk's (NVO) popular weight-loss drug semaglutide, also known as Ozempic and Wegovy, are suing the FDA for removing the GLP-1 medication from its shortage list. The Outsourcing Facilities Association,

Becker's Hospital Review · 10h

FDA sets deadline to end sales of Ozempic, Wegovy copycats

Compounding pharmacies and telehealth companies selling lower-cost versions of Novo Nordisk's Ozempic and Wegovy will soon have to halt production after the FDA set deadlines to phase out compounded semaglutide.

FDA, recall and Nationwide

Newsweek on MSN · 11h

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 · 9h

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 · 5h

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.

Parkinson's, FDA and Medtronic

Hosted on MSN · 3h

FDA Approves Adaptive Deep Brain Stimulator for Parkinson's Disease

The FDA approved adaptive deep brain stimulation (DBS) technology (BrainSense adaptive DBS and BrainSense electrode identifier) for people with Parkinson's disease, Medtronic announced Monday. Like other DBS devices,

Reuters · 12h

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.

Business Insider · 12h

Medtronic’s BrainSense brain stimulation system approved by FDA for Parkinson’s

Medtronic (MDT) announced FDA approval of BrainSense Adaptive deep brain stimulation – aDBS – and BrainSense Electrode Identifier. There is no

5hon 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 ...

10h

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.

STAT9h

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.

11h

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 ...

11h

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 ...

16hon MSN

NY lawmaker introduces bill to ban Zyn, other flavored nicotine pouches after FDA's support of product

A New York state lawmaker is proposing a ban on the sale of flavored nicotine pouches, even after the FDA authorized the ...

Hosted on MSN45m

Next Science sinks after FDA warning letter implies product could have caused injury

Next Science (ASX:NXS) shares fell -13% on Tuesday morning trades, to 10cps, after the company revealed it’s received a ...

Newser on MSN1h

FDA Change on Ozempic to Shake Up the Market

The shortage of Ozempic and Wegovy has been declared over by the Food and Drug Administration, a change that suggests higher ...

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FDA rehires staff to its medical devices division

Listeria, FDA

Drug compounders sue FDA over semaglutide status

FDA, recall and Nationwide

Parkinson's, FDA and Medtronic

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