President Trump is reportedly set to nominate White House domestic policy aide Heidi Overton as FDA commissioner, placing a conservative physician with ties to Marty Makary and the America First Policy Institute at the head of the agency.
A recall of nearly 1.6 million dozen eggs has been elevated to the FDA's highest-risk warning as a salmonella outbreak sickens at least 98 people across 17 states, resulting in 26 hospitalizations.
美國FDA宣布，中西部家禽服務公司自願召回約1900萬顆可能受腸炎沙門氏菌污染的雞蛋，存在導致嚴重健康風險甚至死亡的風險，特別對幼童、老人及免疫力較弱者。
FDA officials inspected Taylor Farms' processing facility and fields in Mexico as part of an investigation into a nationwide cyclospora outbreak linked to shredded lettuce.
ABD'de 17 eyalette Salmonella salgını nedeniyle 98 vakaya ulaşıldı. 26 hasta hastaneye kaldırıldı, can kaybı olmadı. Üretici firma yumurta dağıtımını durdurdu.
Recent salmonella and cyclosporiasis outbreaks linked to Mexican produce imported by Taylor Farms have exposed critical failures in U.S. food safety and FDA oversight amid declining agency staffing and foreign inspections.
The Bombay High Court told the Maharashtra FDA to use its powers judiciously after Cadila Pharmaceuticals challenged a ban on the sale of some medicines, prompting the regulator to agree to revoke orders and issue show-cause notices.
An FDA report reveals that only 2.5 percent of Cyclospora-tainted lettuce from Taylor Farms went to Taco Bell, while Walmart received over 46 percent amid an outbreak sickening over 23,000 people.
The FDA approved Moderna's mRNA-based seasonal influenza vaccine, mFLUSIVA, for adults 50 and older. It is the first flu vaccine using COVID-19 shot technology and will be available in weeks.
The FDA has approved Moderna's mRNA-based influenza vaccine, mFLUSIVA, for US adults aged 50 and over, marking the first mRNA flu vaccine authorized in the US, leveraging technology from the Covid-19 pandemic.
La FDA a approuvé le vaccin antigrippal à ARNm de Moderna, mFLUSIVA, pour les adultes de 50 ans et plus, après un processus d'examen révisé.
Zyn nicotine pouches received recent FDA authorization to advertise as lower-risk alternatives to cigarettes, dividing public health experts over their harm reduction potential for adult smokers versus the rising appeal and risks for adolescents.
Zimax, sản phẩm của Vivadent, ứng dụng phôi sứ Argen (Mỹ) đạt chứng nhận FDA, cung cấp giải pháp phục hình răng sứ với thẩm mỹ tự nhiên, độ bền cơ học cao và an toàn sinh học.
The FDA is set to decide on Moderna's mRNA flu shot by Wednesday, a ruling with major implications for mRNA research. This follows the agency's initial rejection and subsequent agreement to review the application, causing concern among investors and researchers, especially after HHS cut mRNA vaccine funding.
The FDA regulates sunscreen as an OTC drug, deeming only zinc oxide, titanium dioxide, and bemotrizinol as "generally recognized as safe and effective" (Grase). Experts advise avoiding parabens and phthalates, but emphasize that not using sunscreen poses a greater health risk than using regulated chemical sunscreens.
An FDA committee, stacked with Kennedy-appointed members, voted to lift restrictions on manufacturing four peptides for human use, despite lacking safety and efficacy data, with decisions on three more peptides pending.
An FDA committee voted to recommend six peptides for inclusion on a list that would let compounding pharmacies dispense them, despite FDA staff objections. Critics said the move could widen access to inadequately studied drugs.
An FDA advisory panel narrowly recommended reclassifying four peptides (BPC-157, KPV, TB-500, MOTs-C) to allow compounding pharmacies to dispense them, despite FDA scientists' safety concerns. The decision could move popular, influencer-backed peptides from an unregulated gray market into regulated medical use, sparking debate among experts.
An FDA panel endorsed unproven peptides, Meta's AI ad uses a song about the world ending, EU fines Google $1B for prioritizing its services, and more in tech and policy news.
FDA health advisors voted 8-6 to recommend expanding public access to BPC-157, a popular peptide promoted by HHS Secretary Robert F. Kennedy Jr., despite scientific skepticism about its safety and efficacy. The panel is expected to vote on six other peptides Friday.
The FDA announced its sixth Cyclospora outbreak investigation this year, with 72 new cases, contributing to over 11,500 total cases nationwide. This surge, already exceeding annual norms, follows a previous outbreak linked to Taylor Farms lettuce from Mexico, raising concerns about public health and agency capacity.
Midwest Poultry Services has voluntarily recalled nearly 1.6 million dozen white and brown cage-free shell eggs produced in Texas due to potential Salmonella Enteritidis contamination, distributed to multiple states. Consumers are advised to avoid these eggs.
Nearly 1.6 million dozen eggs from Midwest Poultry Services are recalled across five US states due to potential Salmonella contamination. This recall coincides with a major cyclosporiasis outbreak linked to contaminated lettuce, affecting thousands nationwide, raising concerns about foodborne illnesses.
FDA advisers are meeting for two days to review evidence for seven experimental peptide therapies, including TB-500, BPC-157, and MOTs-C, to determine if they can be compounded by specialized pharmacies despite FDA scientists' recommendations against approval due to limited human data.
