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Pig Kidney Transplant Trials Given FDA Approval in US
FDA OKs clinical trials for pig kidney transplants in people
The U.S. Food and Drug Administration 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.
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.
Walmart, Broccoli and FDA
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
ALERT: FDA Escalates Walmart Broccoli Recall to Top Danger Level in 20 States Over Listeria Scare
The FDA has upgraded a broccoli recall to Class I due to potential Listeria contamination in Walmart-sold products.
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.
FDA, Recalls
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.
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.
Dog food recalled over salmonella risk: Here’s what the FDA wants you to know
Healthy people infected with salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and
Acrivon Therapeutics, FDA and Breakthrough Device
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,
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.
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.
17h
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 ...
Healio
1h
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 ...
1h
on 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 NY1
16h
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 ...
Pharm Exec
2h
FDA Grants Fast Track Designation to Adicet Bio’s CAR T-cell Therapy for Systemic Lupus Erythematosus
The FDA has granted Fast Track Designation to Adicet Bio’s ADI-001, an allogeneic gamma delta CAR T-cell therapy, for ...
4h
FDA Accepts Integral Molecular's Membrane Proteome Arrayâ„¢ Qualification Plan, Advancing the Platform for Approval as a Drug Development Tool
Integral Molecular, a leader in antibody discovery technologies, is proud to announce that the FDA has accepted their Membrane Proteome Arrayâ„¢ (MPA) Qualification Plan for advancement as a Drug ...
MedPage Today
21h
FDA OKs New Wearable Treatment for Parkinson's Disease
The FDA approved an apomorphine hydrochloride infusion device (Onapgo) to treat motor fluctuations in adults with advanced ...
Business Wire
21h
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 ...
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