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9 Feb 2019, 9:43 am
CDC, the Food and Drug Administration (FDA), and state and local health departments initiated a multistate investigation. [read post]
4 Feb 2012, 1:59 am
Food and Drug Administration reported finding low levels of fungicide carbendazim in orange juice headed for U.S. supermarkets, but assured the public the juice remains safe to drink.Of the 14 samples, which were taken from large holding tanks of juice concentrate at large domestic orange juice processors, nine tested positive for carbendazim, five had no measurable level of carbendazim (below 10 parts per billion). [read post]
19 Mar 2017, 9:05 pm
Food and Drug Administration officials led by acting FDA Commissioner Stephen Ostroff that they’d be getting the review with the likely delay in compliance. [read post]
26 Apr 2011, 7:15 pm
On April 26, 2011, the Food and Drug Administration (FDA) filed suit against Rainbow Acres Farm in Pennsylvania seeking a permanent injunction to halt the sale of unpasteurized, or "raw" milk. [read post]
27 Feb 2022, 9:05 pm
” In the U.S., the Food and Drug Administration oversees the safety of most of the human and animal food consumed in the United States. [read post]
21 Nov 2019, 3:35 pm
Department of Agriculture (USDA), and the Food and Drug Administration (FDA) investigated a multistate outbreak of 356 Salmonella Reading infections from 42 states and the District of Columbia (DC) linked to turkey. [read post]
26 Jan 2008, 5:00 pm
Drinking raw (untreated) milk or eating raw milk products is "like playing Russian roulette with your health," says John Sheehan, director of the Food and Drug Administration's Division of Dairy and Egg Safety. [read post]
4 May 2018, 9:00 pm
Badger Botanicals LLC of Springville, UT, is recalling four of its kratom products because tests by the Food and Drug Administration returned positive results for Salmonella contamination in the product. [read post]
8 Jul 2011, 2:59 am
Food and Drug Administration guidelines. [read post]
1 Dec 2015, 11:50 am
Xarelto was developed by German pharmaceutical giant Bayer, and is jointly marketed in the United States with Janssen Pharmaceuticals, a division of Johnson & Johnson. [read post]
7 Feb 2019, 9:03 pm
Contributed Editor’s note: Three top Food and Drug Administration officials joined to write this FDA Voices blog, which was originally posted by the agency on Feb. 7, 2019. [read post]
27 Jun 2011, 5:23 pm
In a rare, but refreshing move, the Food and Drug Administration (FDA) has issued a warning to consumers to avoid eating Evergreen Produce brand alfalfa sprouts or spicy sprouts because they may be linked to 20 cases of Salmonella poisoning. [read post]
1 Jun 2014, 10:01 pm
Department of Agriculture and the Food and Drug Administration. [read post]
29 Dec 2015, 10:03 pm
Food and Drug Administration (FDA) and respond to Congressional concerns about duplication of efforts between USDA and FDA. [read post]
21 Aug 2023, 7:47 am
Cohen is a member of the Administrative Conference of the United States. [read post]
27 Jan 2012, 1:59 am
Food and Drug Administration established a policy in 1992 declaring that there is no substantial or material difference between genetically engineered foods and foods that haven't been genetically engineered.While genetically modified foods may be relatively safe by science-based approaches to risk assessment, the issue of labeling GMO foods is about public confidence. [read post]
21 Sep 2021, 9:05 pm
Drugs of abuse — The Department of Justice’s Drug Enforcement Administration (DEA) works to enforce the controlled substances laws and regulations of the United States, including as they pertain to the manufacture, distribution, and dispensing of legally produced controlled substances. [read post]
10 Oct 2023, 4:00 am
The Food and Drug Administration recently updated the warning label on Horizon Pharmaceutical’s TEPEZZA. [read post]
8 Jul 2013, 1:35 pm
Mensing case decided by the Supreme Court of the United States in 2011 (the so-called "Mensing ruling"), which is explained in these earlier posts: March 2012 Update: Generic Drug Manufacturers Immunity By Means Of Mensing Preemption RulingPublic Citizen Group Files FDA Petition To Fix Problems Exposed By Mensing Case Ruling Generic Drug Company Should Not Be Allowed To Use Federal Preemption To Defeat Lawsuits Returning to that July 3 New York Times article… [read post]
29 Mar 2019, 10:20 am
When a drug proves safe and effective, the drug company applies to the Food and Drug Administration (FDA) for a license to manufacture and produce the new drug. [read post]
