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More Than 4 Million Eggs Are Part of a Class 1 Recall by FDA

FDA says egg recall over salmonella can have 'serious' health effects: Avoid these brands

Eggs sold in three states have been recalled due to possible salmonella contamination. Here's what consumers need to know about symptoms, brands and more.

as.com · 9m

FDA recalls over 4 million eggs: how to know you purchased contaminated eggs

It doesn’t matter the size, egg type, or expiration date, says the FDA; all eggs fall under the recall. Samples taken from the hen house and the processing facility matched the strains identified in the lab testing done by the CDC on the infected patients.

FOX News on MSN · 1d

Consumers asked to throw away millions of eggs as FDA upgrades recall status to most serious category

The FDA announced that the recall of "Milo’s Poultry Farms" and "Tony’s Fresh Market" has been upgraded to Class I, meaning the eggs may cause serious health issues or death.

FDA approves 1st flu and COVID-19 combo home test

ConsumerAffairs · 1h

FDA approves first combo flu-COVID-19 at-home test

The Food and Drug Administration (FDA just approved a new at-home test that can tell you if you have COVID-19 or the flu. You can buy it without a prescrip

ABC · 1d

FDA authorizes 1st over-the-counter combo flu and COVID test outside of emergency use

The FDA has authorized the first over-the-counter combination COVID-19 and flu test outside of emergency use, which delivers results at home in about 15 minutes.

MarketWatch · 1d

FDA Authorizes Marketing of First Home Flu and COVID-19 Combination Test Outside of Emergency Use Authorities

Today, the U.S. Food and Drug Administration granted marketing authorization for the Healgen Rapid Check COVID-19/Flu A&B Antigen Test. The test, authorized for use without a prescription, is for use by individuals experiencing respiratory symptoms and uses a nasal swab sample to deliver at-home results in approximately 15 minutes for COVID-19 and influenza (flu).

FDA, Phases of clinical research

STAT · 11h

Q&A: How the FDA is approaching AI in clinical trials and drug development

The FDA's Tala Fakhouri discusses the agency's approach to the regulation of AI in clinical trials in a new interview.

Business Insider · 8h

Ocugen: FDA Lifts Clinical Hold On Investigational New Drug Application For Phase 1 Trial Of OCU200

Ocugen (OCGN) reported that the FDA has lifted the clinical hold on the investigational new drug application for the Phase 1 clinical

MarketWatch · 9h

Ocugen Says FDA Lifts Clinical Hold on Diabetic Macular Edema Drug

Ocugen said the Food and Drug Administration lifted a clinical hold on its OCU200 investigational treatment for diabetic macular edema, paving the way for Phase 1 trials. The Malvern, Penn., biotechnology company Wednesday said trials will include three cohorts to assess the safety of OCU200,

Boehringer, FDA and Zealand

Reuters on MSN · 1d

Zealand, Boehringer win FDA breakthrough status to treat fatty liver

Denmark's Zealand Pharma and German partner Boehringer Ingelheim have won the U.S. Food and Drug Administration's Breakthrough Therapy for the review of their experimental weight-loss drug for the treatment of a type of fatty liver disease.

Business Insider · 19h

Zealand : Boehringer Gets FDA Breakthrough Therapy Designation For Survodutide In Non-Cirrhotic MASH

Zealand Pharma A/S (ZEAL) reported that Boehringer Ingelheim announced that the U.S. Food and Drug Administration has granted

GlobalData on MSN · 1d

Boehringer kickstarts two Phase III trials as MASH therapy wins breakthrough status

Boehringer Ingelheim has received a breakthrough therapy designation from the US Food and Drug Administration (FDA) for survodutide as a treatment for non-cirrhotic metabolic dysfunction-associated steatohepatitis (MASH) and moderate or advanced fibrosis.

MedPage Today8m

FDA Reviewers Cast Doubt on Drug Candidate for Barth Syndrome

In its new drug application, Stealth BioTherapeutics described elamipretide as a first-in-class mitochondrial protective ...

59mon MSN

Eggs sicken 2 in California as FDA bumps recall up to highest threat level

California has been linked to a Food and Drug Administration recall of 4 million eggs. On Sept. 6, the Center for Disease ...

21h

US FDA declines to approve Zealand's drug for low blood sugar in infants

The U.S. health regulator has declined to approve Zealand Pharma's drug to prevent and treat low blood sugar in children with ...

Vendors of Synthetic Nicotine Vapes on Instagram Are Skirting FDA Rules

Spurred on by that knowledge, the FDA in 2022 mandated that all synthetic nicotine vape products "include a health warning ...

6hon MSN

Bakery that makes Sarah Lee and Entenmann's breads pushes back on FDA sesame warning

A top U.S. commercial bakery is pushing back on a Food and Drug Administration warning to stop using labels that say its ...

1don MSN

Vegetable Recall Update: Warning for State As FDA Sets Highest Risk Level

The vegetable products were recalled due to a possible contamination with the bacteria Listeria monocytogenes.

STAT14h

Compounding group sues FDA for removing Lilly’s obesity drug from its shortages list

A trade group representing compounding pharmacies sued the FDA for a “reckless and arbitrary” decision to remove Eli Lilly's ...

15hon MSN

WeightWatchers offering compounded version of Ozempic, despite concerns expressed by FDA

High demand has created a market for compounded versions of the drug best known as Ozemic or Wegovy, but doctors and the FDA ...

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