fda food and drug administration

FDA labels broccoli sold at Walmart

NJ.com · 14h

Broccoli recall: FDA upgrades recall to ‘deadliest level’ for florets sold at Walmart in 20 states, throw out ASAP

The recall announced in January involves contaminated broccoli sold in 20 states. Here's everything you need to know

Yahoo · 1d

FDA labels broccoli sold at Walmart as deadly. See where it was sold and what you should do

The U.S. Food and Drug Administration has labeled the broccoli recall as a Class I, the highest risk level issued by the agency.

6abc News · 12h

Recalled broccoli sold at Walmart labeled potentially deadly by FDA

Braga Fresh Foods initially issued a voluntary recall for one lot of its 12-ounce bags of Marketside Broccoli Florets on Dec. 27, 2024, according to the original company announcement shared by the FDA on Dec. 31, 2024.

USA Today · 1d

FDA labels broccoli sold at Walmart as deadly. See what California stores sell it

The U.S. Food and Drug Administration has labeled the broccoli recall as a Class I, the highest risk level issued by the agency.

Houston Chronicle on MSN · 7h

FDA upgrades recalled broccoli to highest level over possible Listeria contamination

The U.S. Food and Drug Administration upgraded the classification of recalled broccoli sold at Walmart originally issued in December to its highest recall category, according to the agency’s updated report.

Acrivon Therapeutics, FDA

Business Insider · 18h

Acrivon Therapeutics announces FDA granted BDD for ACR-368

Acrivon Therapeutics (ACRV) announced the U.S. Food and Drug Administration, FDA, has granted Breakthrough Device designation, BDD, for the

MarketWatch · 19h

Acrivon Therapeutics Gets FDA Breakthrough Device Designation for Cancer Identification

Acrivon Therapeutics said the Food and Drug Administration has granted Breakthrough Device designation for its ACR-368 OncoSignature assay, an immunofluorescence assay for the identification of endometrial cancer patients who may benefit from ACR-368 treatment.

Investing.com on MSN · 17h

ACR-368 OncoSignature assay gains FDA breakthrough status

Acrivon Therapeutics, Inc. (NASDAQ: ACRV), a clinical stage biopharmaceutical company with a market capitalization of $184 million and an impressive 60% stock return over the past year, announced that its ACR-368 OncoSignature assay has received Breakthrough Device designation from the U.

1don MSN

U.S. FDA approves Supernus' drug-device combination for Parkinson's disease

The U.S. Food and Drug Administration has approved Supernus Pharmaceuticals' drug-device combination to treat ...

Insurer Denies Access To Drugs Granted Accelerated Approval By FDA

Going forward, we may see more instances in which insurers deny or (temporarily) severely restrict coverage of accelerated ...

HealthDay on MSN10m

FDA Approves Symbravo for Acute Treatment of Migraine in Adults

WEDNESDAY, Feb. 5, 2025 (HealthDay News) -- The U.S. Food and Drug Administration has approved Symbravo (meloxicam and ...

15hon MSN

Novo Nordisk Expects Positive News on Weight-Loss Drugs, Soon, From FDA

The drugmaker expects the regulator to remove Wegovy and Ozempic from its shortage list, blocking other companies from ...

5don MSN

FDA approves first new non-opioid painkiller in decades, and it's from a MA company.

The U.S. Food and Drug Administration approved a new non-opioid pain medication developed by the Massachusetts-based company ...

US FDA approves Axsome Therapeutics' migraine drug

The U.S. Food and Drug Administration has approved Axsome Therapeutics' migraine treatment, the company said on Thursday.

Business Wire1d

FDA Approves Genentech’s Susvimo as the First and Only Continuous Delivery Treatment for the Leading Cause of Diabetes-Related Blindness

Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY) announced today that the U.S. Food and Drug ...

16hon MSN

What Is Front-of-Package Food Labeling? And Will it Help?

The FDA says new labels will make it easier to spot harmful ingredients. A UVA nutritionist suggests taking a holistic ...

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