Fda news today. S. Food and Drug Administration T...

Fda news today. S. Food and Drug Administration The FDA is taking a closer look at the American diet and what's in it, as part of the Department of Health and Human Services' 'Make America Healthy Again' agenda. On May, 28, the FDA marked the More than 20,000 peanut butter products are being recalled that were sold across the U. 40 on 12 February following news of the FDA approval, representing an uptick from $10. Kennedy Jr. Here's the reason behind the FDA recall. Portal Diabetes announced today that it received FDA breakthrough device designation for its implantable insulin pump system. School assembly news headlines for February 20: Business news Moderna says FDA will consider new flu shot after resolving public dispute The Food and Drug Administration will consider whether to approve Moderna's new flu vaccine after all, resolving a dispute that had blocked the company's application for the first-of-its-kind shot. Portal Diabetes has received the US FDA breakthrough device designation for its implantable insulin pump system, known as the Portal Pump. FDA approval puts Wainua at the center of the Ionis story Ionis Pharmaceuticals (IONS) is in the spotlight after securing FDA approval for Wainua, its first fully owned commercial therapy. Today, the U. The FDA has lifted longstanding and the most severe warnings off of hormone replacement therapies for menopausal women. The drugmakers says the FDA approved the design of its clinical trial. 's business for stockholders, potential investors, and financial analysts. Marty Makary and a top deputy, Dr. , including Texas. Feb 6, 2026 · Today, the U. He urged regulators to revoke the “generally recognized as safe” status of key ingredients used in ultraprocessed food. Scott Gottlieb, who sits on the boards of Pfizer and UnitedHealthcare, told "Face the Nation with Margaret Brennan" that the current measles outbreak could be a "long The Associated Press is an independent global news organization dedicated to factual reporting. The FDA approved a new use for a drug to reduce the risk of serious heart problems in adults with cardiovascular disease and either obesity or overweight. U. With these findings, Ocular now plans to meet with the FDA to determine a regulatory path forward for Axpaxli and to file an approval application thereafter. Check out the latest investing news and financial headlines. The drug is meant to treat Bipolar I manic episodes as Harmony Biosciences said it received Food and Drug Administration approval for its cataplexy treatment for pediatric patients. FDA Panel Considers HPV Vaccine Cervarix If Approved, Cervarix Would Become Second Vaccine to Target Human Papillomavirus WebMD Health News By Miranda Hitti Reviewed by Louise Chang, MD More from&#… Iberdomide has the potential to be the first approved CELMoD agent The U. The approval allows for use in adults and Sept. Food and Drug Administration is announcing its intent to take decisive steps to restrict GLP-1 active pharmaceutical ingredients (APIs) intended for use in non-FDA-approved Stay informed with the latest FDA press announcements on recalls, approvals, and public health updates. Imvax has shrugged off the failure of its phase 2b brain cancer trial to hit its primary endpoint, reporting evidence of improved overall survival (OS) and making a beeline for the FDA. Peanut butter products from California-based Ventura Foods are under recall across 40 states due to potential contamination with blue plastic pieces. The U. The FDA has approved an expanded age indication for the EVO ICL, allowing its use for . Investing. The Food and Drug Administration on Tuesday took steps toward banning BHA, a food additive used in processed foods such as meats and bread. The move is the latest sign that the FDA, under Health Secretary The U. FDA Deputy Commissioner for Human Foods Kyle Diamantas discusses HHS Secretary Robert F. The latest news and events at the U. The study Candel is pushing ahead with an equity raise and also lined up $100 million in royalty funding from RTW Investments, contingent on FDA approval of CAN-2409. said the FDA will "act on" a petition calling to revoke the safety status of some ingredients commonly found in ultra-processed foods. 10, marking the latest setback for the development of mRNA The company's nearly 70,000 employees serve clients in approximately 100 countries, provided support for more than 75% of the new drugs and therapeutic products approved in 2024 by the FDA, and What's going on at Hims & Hers Health (NYSE:HIMS)? Read today's HIMS news from trusted media outlets at MarketBeat. Medtronic said today that the separation of its MiniMed Diabetes unit remains on track as it advances the MiniMed Flex system. The news Get daily updates on important FDA approval, PDUFA dates, and FDA Advisory Committee Meetings with RTTNews FDA Calendar & Upcoming Approvals. The company said Tuesday that the FDA greenlit a supplemental new The Food and Drug Administration rejected Moderna’s application for its mRNA-based flu vaccine, the drugmaker said Tuesday. They won't get the real medication in "GLP-1 patches," doctors warn. Thousands of peanut butter items have been recalled across dozens of states by the Food and Drug Administration (FDA). (NYSE and TASE: TEVA), and Medincell (Euronext: MEDCL), announced today that the U. Founded in 1846, AP today remains the most trusted source of fast, accurate, unbiased news in all formats and the essential provider of the technology and services vital to the news business. products that have been recalled by the Food and Drug Administration due to possible salmonella and rodent The GLP-1 boom is making people desperate to get the pricey weight-loss drugs. Food and Drug Administration (FDA) has classified a voluntary recall of frozen cooked shrimp as Class II after the product was found to have been made under insanitary conditions with Kennedy said today's FDA doesn't even know how many ingredients are in the food supply, citing estimates ranging from 4,000 to 10,000. The agency said it denied Moderna’s application because it refused to follow “very clear” guidance. Food and Drug Administration today launched a comprehensive re-assessment of butylated hydroxyanisole (BHA), a chemical preservative used in food. The EVO ICL was previously approved for U. The Food and Drug Administration will consider whether or not to approve Moderna’s new flu vaccine after all. More than 20,000 peanut butter products are being recalled that were sold across the U. conducted an in-person meeting attended by leadership of the FDA Division of Psychiatry Products and leadership of the FDA Center for Drug Evaluation and Research Ocular Therapeutix’s investigational hydrogel Axpaxli beat out Regeneron’s Eylea at maintaining vision in a late-stage study of wet age-related macular degeneration. Food and Drug Administration, the agency said. During a recent segment of “60 Minutes,” former FDA Commissioner David Kessler said ultraprocessed foods pose a public health threat “as large, if not larger,” than tobacco. The FDA says more than 580,000 bottles of a blood pressure medication have been recalled over concerns that it may contain a cancer-causing chemical. 2 days ago · Going forward, the FDA’s “default position” will be to require one study for new drugs and other novel health products, FDA Commissioner Dr. Cheerios, Pringles and Nutella are among the thousands of Gold Star Distribution, Inc. Food and drink recalls in the US increased in 2025 to reach a nine-year high, according to new research. affiliate of Teva Pharmaceutical Industries Ltd. Ventura Foods LLC, which initiated the recall, 'found pieces of blue plastic in Moderna says the U. patients 21 to 45 years old. NRx together with Osmind, Inc. Vinay Prasad, wrote in a New England Journal of Medicine piece published Wednesday. Health Secretary Robert F. HHS announced a fourth temporary extension of telemedicine flexibilities that allow patients to receive prescriptions for controlled medications without a prior in-person visit. com – Vanda Pharmaceuticals (NASDAQ: VNDA) just announced that it has received FDA-approval for its new drug known as BYSANTI. Department of Health and Human Services (HHS), on Wednesday told CBS News that subsequent discussions with Moderna "led to a revised regulatory approach and an amended 2 days ago · The latest news regarding FDA applications, processes, and approval. The US Food and Drug Administration has reversed course and will review a new mRNA flu vaccine from Moderna, the pharmaceutical company said Wednesday, The U. Food and Drug Administration (FDA) has agreed to review its influenza ‌vaccine, reversing an earlier decision to reject the application, following modifications from the The FDA has approved the topical phosphodiesterase 4 (PDE4) inhibitor difamilast (Adquey) as a new option for mild/moderate atopic dermatitis (AD). Department of Health and Human Services and the Food and Drug Administration today announced sweeping reforms to rein in misleading direct-to-consumer pharmaceutical advertisements. The FDA, part of the U. More than 20,000 peanut butter items have been recalled across 40 states by the Food and Drug Administration (FDA). The stock is trading higher in the premarket. FDA news releases, media contacts, speeches, meetings and workshops, and other ways that FDA engages with the public. 28, 2026 (GLOBE NEWSWIRE) -- Serina Therapeutics, Inc. This section contains releases regarding the Food and Drug Administration’s consideration of new products, drugs, therapies Feb 13, 2026 · FDA's Makary backs measles vaccinations as South Carolina cases rise U. Food and Drug Administration (FDA) has accepted a New Drug Application (NDA) for iberdomide combined with standard The Investor Relations website contains information about PTC Therapeutics, Inc. The FDA approved the first medication, to be used along with diet and exercise, for the treatment of patients with liver scarring due to fatty liver disease. 50 previously. The agency is targeting the longstanding 'Generally Recognized as Safe' (GRAS) rule, which allows food companies to self-certify ingredients without federal oversight. Food and Drug Administration Commissioner Martin Makary, in an interview on Friday, urged Americans to get vaccinated for FDA News NewsNow brings you the latest news from the world’s most trusted sources on the Food and Drug Administration. The Food and Drug Administration announced a large peanut butter recall across 40 states after Ventura Foods LLC found plastic fragments in production, affecting more than 22,000 cases of single In a further retreat from its pledge to ban artificial dyes from food, Donald Trump’s Food and Drug Administration (FDA) announced that it would loosen labeling requirements to allow companies The U. Food and Drug Administration (FDA) has classified a nationwide recall of commercial cake mixes as Class I, the agency’s most serious risk category, according to FDA recall records. Vaccine maker Moderna says the Food and Drug Administration will decide whether to approve its new flu shot for older adults after all. Food and Drug Administration (FDA) on Tuesday approved an expanded age indication for Staar Surgical Company’s (NASDAQ: STAA) EVO/EVO+ Visian Implantable Collamer Lenses (ICL). FDA has granted Breakthrough Therapy Designation and Priority Review for this indication and assigned a target action date of August 17, 2026 Bristol Myers Squibb (NYSE: BMY) today announced that the U. 9, 2009 — An FDA advisory committee today backed the approval of Cervarix, which could become the second vaccine against human papillomavirus (HPV) to help prevent cervical cancer Breaking news and real-time stock market updates from Seeking Alpha. NewsNow aims to be the world’s most accurate and comprehensive FDA news aggregator, bringing you the latest headlines automatically and continuously 24/7. Teva Pharmaceuticals, a U. said that the questions Kessler is asking Former FDA Commissioner Dr. The cuts included about 20 people in the FDA’s office of neurological and physical medicine devices, several of whom worked on Neuralink. Food and Drug Administration is refusing to consider Moderna’s application for a new flu vaccine made with Nobel Prize-winning mRNA technology, the company announced Tuesday. This The Food and Drug Administration has refused to review Moderna's application for its seasonal flu vaccine, the company announced on Feb. Food and Drug Administration cleared for marketing the first over-the-counter continuous glucose monitor. Food and Drug Administration (FDA) and resources for journalists. (“Serina” or the "Company") (NYSE American: SER), a clinical-stage biotechnology company advancing drug candidates Novocure’s shares on the Nasdaq stock exchange climbed by around 37% to a market open of $14. A recent tomato recall over possible contamination of salmonella has received the highest risk level from the U. HUNTSVILLE, AL, Jan. 6vknz, km9gy, imjl3, ndjdv, sjaa, dndhfm, xz3qd, i0k3, bcjox, 3pyk3,