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3 Jun 2014, 2:24 pm
Recent outbreak just one in a string affecting supposedly “healthy” foods At the end of last month, a nationwide recall was announced by the Food & Drug Administration related to an outbreak of Salmonella Newport connected with chia powder and smoothie mix. [read post]
19 Feb 2009, 7:51 am
The suits, brought under the qui tam provisions of the False Claims Act, allege that the companies engaged in off-label marketing of the drug Natrecor.Drug manufacturers are required to specify the intended use of a drug in their application for approval from the Food and Drug Administration. [read post]
11 Dec 2019, 11:31 am
Food and Drug Administration issued a revised consumer alert on Cannabidiol (CBD), warning that the agency is aware that some companies are marketing CBD products in ways that violate the federal Food, Drug and Cosmetic Act (FD&C Act), and that may put the health and safety of consumers at risk. [read post]
11 Dec 2019, 11:31 am
Food and Drug Administration issued a revised consumer alert on Cannabidiol (CBD), warning that the agency is aware that some companies are marketing CBD products in ways that violate the federal Food, Drug and Cosmetic Act (FD&C Act), and that may put the health and safety of consumers at risk. [read post]
25 Apr 2012, 9:30 am
Public Notification: "ZenMaxx" Contains Undeclared Drug Ingredient The Food and Drug Administration (FDA) is advising consumers not to purchase or use "ZenMaxx," a product for sexual enhancement manufactured by Enhance Nutraceutical, and sold on various websites, including www.zenmaxx.com. [read post]
12 Aug 2008, 8:10 pm
Food and Drug Administration is warning consumers who filled prescriptions at The Medicine Shoppe pharmacies located at 8035A Liberty Road and 5900 Reisterstown Road in Baltimore that they may have received drugs that were either expired or suspected counterfeit. [read post]
1 Mar 2023, 9:05 pm
The Food and Drug Administration reports that it has begun product traceback efforts, but the agency has not named the product or products being traced. [read post]
14 Jul 2012, 2:41 pm
States Food & Drug Administration (FDA) issued a notice in the Federal Register directing companies to discontinue manufacturing and distributing particular unapproved drugs that contain oxycodone. [read post]
14 Jul 2012, 2:41 pm
States Food & Drug Administration (FDA) issued a notice in the Federal Register directing companies to discontinue manufacturing and distributing particular unapproved drugs that contain oxycodone. [read post]
27 Mar 2012, 11:37 am
Leon found that the Food, Drug, and Cosmetics Act didn’t give the FDA discretion to allow shipments of the unapproved drug. [read post]
13 Aug 2010, 2:59 am
Food and Drug Administration (FDA) about "serious violations" of federal laws and regulations for imported fish.FDA said, "there must be evidence that all fish and fishery products offered for entry into the United States have been processed under conditions that comply with 21 CFR Part 123. [read post]
3 Apr 2020, 8:31 am
The Food and Drug Administration (FDA) closely regulates drugs and takes steps to protect public safety if any issues are discovered. [read post]
20 Nov 2023, 12:47 am
Food and Drug Administration (FDA) are collecting different types of data to investigate a multistate outbreak of Salmonella Thompson infections. [read post]
23 Mar 2020, 9:03 pm
Food and Drug Administration if they want a piece of the U.S. market, and once again foreign food producers outnumber the domestic ones. [read post]
27 Aug 2014, 10:02 pm
Food and Drug and Administration’s new food safety regulations aren’t the only changes facing fresh produce marketers, but the coming rules likely will be the most far-reaching, Robert Brackett believes. [read post]
30 Jun 2014, 10:04 pm
Food and Drug Administration (FDA) posted seven warning letters in the past week consisting of warnings to five dairies — all for drug residue issues — and to two seafood processors for insanitary conditions. [read post]
13 Nov 2017, 1:46 pm
Food and Drug Administration (“FDA”) Commissioner Scott Gottlieb spoke as a keynote speaker at the Federal Trade Commission (“FTC”) workshop, Understanding Competition in Prescription Drug Markets: Entry and Supply Chain Dynamics (“Workshop”) and called to “end the shenanigans” that can delay or restrict generic drug competition. [read post]
30 Jan 2009, 8:08 pm
The Food & Drug Administration is coming under new scrutiny for not appropriately vetting doctors who try out medications prior to FDA approval. [read post]
12 May 2011, 2:59 am
Food and Drug Administration seized food at American Mercantile, a Tennessee company whose website says it is a "worldwide importer, exporter, dealer and processor of bulk natural products including spices, seeds, herbs, botanical, extracts, essential oils, natural pigments, sweeteners and raw materials. [read post]
4 Dec 2013, 10:10 am
Serious skin reactions medically known as Stevens-Johnson Syndrome (SJS) and toxic epidermal necrolysis (TEN), can occur at any time during Onfi treatment warns the Food and Drug Administration. [read post]
