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FDA, Walmart and Broccoli

NJ.com · 2h

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

Rolling Out · 3h

FDA warns of deadly risk in Walmart frozen broccoli

Nationwide health alert over listeria risk leads to major Walmart broccoli recall affecting 35,508 bags across 20 states as FDA warns of potential deadly consequences.

Fox Business · 2d

FDA escalates Walmart broccoli recall to highest threat level: Risk of 'death'

Some packages of Walmart-sold broccoli florets have been recalled by its manufacturer. The FDA has designated the recall as a Class I, the most serious category.

FDA approves studies of pig organ transplants

The Washington Post on MSN · 1d

FDA approves pig organ transplant trials for patients with kidney failure

The first clinical trials using organs from genetically modified pigs offer hope to patients with kidney failure, who face a long wait for human organ transplants.

U.S. News & World Report · 1d

FDA Approves Clinical Trials for Pig Kidney Transplants in Humans

TUESDAY, Feb. 4, 2025 (HealthDay News) -- The U.S. Food and Drug Administration (FDA) has approved the first-ever clinical trials testing pig kidney transplants in people with kidney failure, marking a major step forward in cross-species transplantation.

Bloomberg L.P. · 1d

FDA Greenlights Studies of Pig Kidney Transplants in Humans

The US Food and Drug Administration approved clinical trials that will transplant organs from genetically modified pigs into patients with kidney failure.

Acrivon Therapeutics, FDA and Breakthrough Device

Business Insider · 4h

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 · 7h

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 · 5h

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.

19hon MSN

Supplement Recall Update as FDA Sets Highest Risk Level

A weight loss supplement has been given the FDA's highest recall classification after being pulled from shelves in December.

18h

FDA is recalling more than 32,000 packages of these popular breadcrumbs sold nationwide

The California-based company has recalled 26,400 eight-ounce packages of its Unseasoned Bread Crumbs (Pan Rayado) and 6,240 ...

Healio3h

FDA grants 510(k) clearance to AI Optics’ handheld retinal imaging system

The FDA has granted 510(k) clearance to AI Optics’ Sentinel Camera, a handheld retinal imaging system that captures ...

20hon MSN

Nut Recall Update for 8 States As FDA Sets Risk Level

A pecan nut product that was recalled due to undeclared walnuts has been given a Class II classification by the food agency.

What FDA Recalls In 2024 Taught Us About Food And Consumer Trust

From mislabeled allergens to major contamination scares, each incident was a reminder of how deeply food safety is woven into ...

1hon MSN

FDA advises diabetes device users to check alert settings

The FDA is advising users of diabetes devices that rely on smartphones to deliver safety alerts to regularly check their ...

3hon 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 ...

Spectrum News NY118h

Doctors for America sues CDC, FDA to restore health data removed from websites

The health care advocacy group said removing health information to comply with Trump's executive orders worsens medical care ...

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FDA, Walmart and Broccoli

FDA approves studies of pig organ transplants

Acrivon Therapeutics, FDA and Breakthrough Device

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