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FDA approves studies of pig organ transplants
FDA clinical trial inclusivity guidelines will be back
Following the president’s recent executive order dismantling diversity, equity, and inclusion policies, the main page for the FDA’s Diversity Action Plan guidelines — requiring pharmaceutical companies to test drugs on diverse populations before approval — has been down since Jan. 23.
FDA Approves Clinical Trials for Pig Kidney Transplants in Humans
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.
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.
Broccoli, FDA and Walmart
Broccoli sold at Walmart recalled in 20 states now labeled deadly by FDA
Last year, California-based grocery producer Braga Fresh voluntarily issued a precautionary recall of 12-ounce washed and ready-to-eat Marketside Broccoli Florets sold at more than 1,000 Walmart stores due to the possibility of Listeria monocytogenes contamination.
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.
Broccoli recall hits ‘deadly’ level: Here’s what to know.
The recall level has been elevated to the highest the U.S. Food & Drug Administration (FDA) has, meaning the broccoli may potentially be deadly to susceptible individuals. According to an FDA press release,
1d
on MSN
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 ...
Targeted Oncology
16h
FDA Grants Key Oncology Approvals and Designations in January 2025
On January 7, 2025, the FDA granted priority review to the new drug application for sunvozertinib (DZD9008), an oral EGFR ...
14h
Updated drug information handout outdoes FDA's version in clinical trial
A clinical trial comparing a one-page medication handout proposed by the U.S. Food and Drug Administration (FDA) with an ...
10h
FDA clears migraine device for children as young as 8
A device long used by adults to manage migraines was now available for children as young as eight years old, offering new ...
dvm360
11h
FDA notifies veterinarians of animal burn risk linked to human medical devices
Following a recall of grounding pads produced by Megadyne, a machinery industry company, the FDA is notifying veterinarians ...
Interesting Engineering on MSN
1d
US FDA approves first-ever smart glasses with hearing aid for mild to moderate loss
EssilorLuxottica's Nuance Audio Glasses receive FDA clearance for OTC sales in the US, revolutionizing hearing solutions with ...
2d
on MSN
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.
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