Food and Drug Administration FDA

Dog food recalled over salmonella risk

Hosted on MSN · 1d

FDA Changes Raise Concerns About Food Recalls

The number of hospitalizations and deaths from foodborne illness doubled last year compared to 2023 in the U.S.

Staten Island Advance · 1d

Dog food recalled over salmonella risk: Here’s what the FDA wants you to know

Blue Ridge Beef is recalling 5,700 pounds of its 2-pound log Natural Mix, according to the FDA, which warned that salmonella can affect animals, and there is risk to humans from handling the food, especially if they have not thoroughly washed their hands after having contact with the product or any surfaces exposed to the it.

Forbes · 1d

Class 1 Recalls & Food Safety—Why They’re More Common Than You Think

Class 1 recalls pose serious health risks, from undeclared allergens to bacterial contamination. Here’s how Class 1 recalls work, plus major FDA food recalls in 2025.

FDA upgrades recalled broccoli to highest level

Hosted on MSN · 4h

FDA Assigns Highest Risk Level To These Recalled Chocolate Snacks

The snacks are now part of a Class I recall, which is for products with the potential of "serious adverse health consequences." Here's what to know.

Houston Chronicle on MSN · 4h

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.

NJ.com · 11h

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

Acrivon Therapeutics, FDA and Breakthrough Device

Business Insider · 13h

Acrivon Therapeutics:FDA Grants Breakthrough Device Designation For ACR-368 OncoSignature Assay

Wednesday, announced that the FDA has granted Breakthrough Device designation for the ACR-368 OncoSignature assay for the treatment of endometrial cancer. The ACR-368-tailored OncoSignature assay is being used to identify patients most likely to respond to the company's lead drug candidate ACR-368 in an ongoing,

MarketWatch · 16h

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 · 14h

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.

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 ...

healthday5h

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 ...

6abc News9h

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.

JD Supra1d

End of an Era: FDA Retires 2017 Interim Policies for Bulk Drug Lists

On January 7, 2025, the US Food and Drug Administration (FDA) issued two parallel guidance documents for the Section 503A and Section 503B bulk ...

WTKR1d

Sell by, use by, or best by? The FDA wants to know when you throw away food

The FDA says millions of tons of food is wasted every year and now they want to better understand how you feel about ...

The Washington Post9d

Americans might finally have to face what’s in their food

(Scott Olson/Getty Images) In the final days of the Biden administration, the Food and Drug Administration proposed ... including the FDA and the Centers for Disease Control and Prevention ...

healthday5h

FDA Approves Susvimo for Diabetic Macular Edema

Susvimo is the first and only FDA-approved treatment shown to maintain vision in people with diabetic macular edema with ...

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 ...

abc272d

Gerber recalls and discontinues baby product due to choking hazard

The U.S. Consumer Product Safety Commission(CPSC) shared that Gerber Products Company has recalled and discontinued one of ...

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