Fda alerts today. FDA analysis has found the products .

Fda alerts today FDA does not endorse either the product or the company. See the full list so far. Lyons Magnus LLC (“Lyons Magnus”) today announced that it is voluntarily recalling 4 oz. FDA analysis has found the products The FDA warned that some people develop severe itching, or pruritus, after stopping long-term use of the antihistamines cetirizine (Zyrtec) or levocetirizine (Xyzal). S. Food and Drug Administration (FDA) updated this list of select chemicals currently under the agency’s review to provide more insight on the status of the FDA’s Domestic and foreign establishments that manufacture, repack, or re-label drug and biologic products, including vaccines, are required to register with the FDA. Feb 5, 2024 · “Today The World” is voluntarily recalling two lots of Sustain herbal dietary supplement capsules and one lot of Schwinnng capsules to the consumer level. Issues Voluntary Nationwide Recall of One Lot of Phenylephrine Hydrochloride Injection, USP, 10 mg/ mL (Pharmacy Bulk . gov. The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the FDA uses science and data to ensure that approved drugs are of a high quality, safe, and effective. I. C. The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the Sep 24, 2025 · Novel Drugs at FDA: CDER’s New Molecular Entities and New Therapeutic Biological Products Drug and Biologic Approval and IND Activity Reports This Week's Drug Approvals Drug Trials Snapshots The Data Dashboard contains data elements from FDA compliance and enforcement data sources, including Inspections, Compliance Actions, Recalls, Imports, and Food Safety Modernization Act programs. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. Food and Drug Administration (FDA) is warning retailers and consumers not to sell or use certain imported cookware that may leach significant levels of lead (Pb) into food. bags of Lay’s Classic Potato Chips that may contain undeclared milk, after being alerted through a consumer Subscribe to Podcasts and News FeedsPodcasts FDA Direct Drug Information Soundcast in Clinical Oncology (D. WASHINGTON - The U. The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the Sep 24, 2025 · Novel Drugs at FDA: CDER’s New Molecular Entities and New Therapeutic Biological Products Drug and Biologic Approval and IND Activity Reports This Week's Drug Approvals Drug Trials Snapshots The Data Dashboard contains data elements from FDA compliance and enforcement data sources, including Inspections, Compliance Actions, Recalls, Imports, and Food Safety Modernization Act programs. CDRH Databases: a listing of databases for such topics as advisory committees, regulations, good practices, medical devices, Premarket Approval (PMA) and Notification (510 (k)), product codes Domestic and foreign establishments that manufacture, repack, or re-label drug and biologic products, including vaccines, are required to register with the FDA. health officials have expanded warnings about a rare heart side effect associated with the two leading COVID-19 vaccines. The FDA approval of the siRNA drug Redemplo caps off a tumultuous 12 months for Arrowhead, whose partnership with Sarepta caused its own stock to drop during the gene therapy maker’s safety troubles this summer. Oct 15, 2025 · The U. Listing of all external Forms both OMB approved and state using ORA forms On August 19, 2025, the U. Food and Drug Administration has learned that some ranitidine medicines, including some products commonly known as the brand-name drug Zantac, contain a nitrosamine impurity called N Nov 20, 2025 · Read news stories about dangerous medical devices and prescription drugs, health studies and pharmaceutical litigation. g. hhs. , indication (s), population (s), dosing regimen (s)] for each of these products, please see the most recently approved Prescribing Information (or FDA does not issue CGMP certificates at the conclusion of an inspection. FDA warns against using specific eye drops from major brands due to potential risk of eye infections. The U. Nov 3, 2025 · To see the FDA-approved conditions of use [e. Learn more about the FDA’s role in reviewing, approving, and monitoring drugs in the latest La FDA es responsable de proteger la salud pública asegurando la seguridad, eficacia y protección de los medicamentos, los productos biológicos y los dispositivos médicos humanos y General information about FDA – its mission, history, organization, partnerships, etc. Search for FDA guidance documents, learn about the laws enforced by FDA, and more. ) FDA Drug Safety Podcasts Guidance Snapshots New Era of Smarter Food Safety Jan 24, 2025 · Home Safety Recalls, Market Withdrawals, & Safety Alerts Provepharm Inc. O. Aug 7, 2024 · Today, FDA issued a proposed administrative order, to address a safety issue related to over-the-counter (OTC) monograph drug products containing acetaminophen. Instead, this dashboard provides the outcomes, including classification and other details, of a firm’s most recent inspection. Prescribing information for FDA News Release FDA Alerts Patients and Health Care Professionals to Nitrosamine Impurity Findings in Certain Metformin Extended-Release Products Agency Continues Investigations of Nitrosamine The FDA on Tuesday and Wednesday posted notices about warning letters sent to companies and a drug safety notice. A consumer advocacy group said the communications pause could still threaten public safety. Lyons ReadyCare and Sysco Imperial Frozen Supplemental Shakes due to the potential for the products to Feb 5, 2025 · The FDA is alerting users of diabetes-related medical devices that smartphones connected to diabetes devices may fail to send critical safety alerts. Please send general questions related to the drug data in these files to the Center for Drug Evaluation and Research, Division of Drug Information: druginfo@fda. Jul 8, 2025 · Mondelēz Global LLC announced today a voluntary recall of four carton sizes of RITZ Peanut Butter Cracker Sandwiches (8-pack, 20-pack, and 40pack cartons of RITZ Peanut Butter Cracker Sandwiches Dec 18, 2024 · December 16, 2024 – Frito-Lay today issued a recall of a limited number of 13 oz. U. May 12, 2025 · The investigation was reopened in April 2025 after FDA investigators found Listeria in environmental samples collected from Fresh & Ready Foods, LLC during a routine surveillance inspection. FDA continues to actively monitor drug availability and is currently working to determine whether the demand or projected demand for each drug in shortage exceeds the available supply. The FDA is advising consumers to throw away and not to buy the ground cinnamon products because samples of products listed in the table were found to contain elevated levels of lead. Drug Enforcement Administration is warning the American public of a sharp increase in the trafficking of 1 day ago · 7 deaths linked to faulty blood glucose monitors as FDA issues safety warning Abbott reports 736 serious injuries associated with certain sensors that may provide 1 day ago · The FDA has expanded its warning about cookware that could contaminate food with lead for a fourth time.