Search for: "United States Food and Drug Administration"
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7 Jun 2012, 11:11 am
Registered food facilities that manufacture, process, pack, or hold food for human or animal consumption in the United States under section 415(a) of the Federal Food, Drug and Cosmetic Act (21 U.S.C. 350(d)) are required to submit an electronic report to the FDA within 24 hours of discovering reportable adulterated food. [read post]
10 Aug 2013, 4:04 pm
Reports indicate that the United States Food and Drug Administration requested that the pharmaceutical manufacturer, Torrent Pharmaceuticals Ltd, recall their recent output of Olanzapine 10 mg tablets as a “precautionary measure” due to the fact that the drug is repackaged in the United States upon delivery from India. [read post]
30 Oct 2011, 3:57 pm
The United States Food and Drug Administration (FDA) has notified medical providers that the warning labels for 5-aplha reductase inhibitor class of drugs should now include new safety information of the increased risk for prostate cancer. [read post]
18 Oct 2010, 9:15 pm
The drug has previously been banned in Europe, and the United States via the Food and Drug Administration is considering banning the drug too. [read post]
8 May 2015, 4:32 pm
Health, there have been 737 recalls of food since January 2014 alone by the Food and Drug Administration. [read post]
6 Nov 2019, 10:24 am
The voluntary recall is a response to a notification by the Food and Drug Administration and the Canadian Food Inspection Agency of a potential contamination with Listeria monocytogenes. [read post]
21 Jan 2015, 8:38 pm
There was a time when the United States Food and Drug Administration (FDA) did not allow drug companies to direct market to individual users, but that ban was lifted a long time ago. [read post]
28 Nov 2022, 9:01 pm
Food and Drug Administration has awarded the University of Maryland’s (UMD) Joint Institute for Food Safety and Applied Nutrition (JIFSAN) with a five-year, $41 million cooperative agreement. [read post]
16 Mar 2021, 9:19 pm
Food and Drug Administration report. [read post]
18 May 2009, 5:00 am
Food and Drug Administration has announced that drug maker Genentech has withdrawn the psoriasis drug Raptiva from the market because of its link to drug related injury, one of which is a fatal brain infection. [read post]
31 May 2019, 12:42 pm
Food and Drug Administration (FDA) has stepped up criminal enforcement where misbranded drugs are being sold online to consumers. [read post]
13 Mar 2014, 12:22 pm
The Food and Drug Administration is considering some very important changes to its internal rules that would help to eliminate a loophole in accountability for defective drugs. [read post]
27 Dec 2010, 1:59 am
Food and Drug Administration (FDA) says.United Taiwan Corporation owns the facility, which produces Sweet Red Beans for export to the United States. [read post]
8 Apr 2009, 5:14 pm
On April 8, 2009, Genetech and the US Food & Drug Administration (FDA) announced a voluntary phased withdrawal of Raptiva (efalizumab) from the U.S. market. [read post]
1 Aug 2016, 2:43 pm
On March 29, 2012 the Food and Drug Administration (FDA) delivered a Class I recall of the two FMC manufactured drugs due to their negative side effects on dialysis patients. [read post]
1 Aug 2016, 2:43 pm
On March 29, 2012 the Food and Drug Administration (FDA) delivered a Class I recall of the two FMC manufactured drugs due to their negative side effects on dialysis patients. [read post]
13 Jun 2022, 1:11 pm
In a complaint filed May 20, the United States alleged that Edge Pharm Inc., and its owners and operators Marc Chatoff and Kurt Radke, violated the FDCA by manufacturing and distributing adulterated and misbranded drugs, by causing drugs to becoming adulterated and misbranded while held for sale, and by introducing new unapproved drugs into interstate commerce. [read post]
23 Jul 2021, 10:13 am
Nonprofit activist group, STOP Foodborne Illness, has announced that the organization has finalized recommendations to the Food and Drug Administration (FDA) to modernize the nation’s food recall system. [read post]
30 Dec 2020, 6:33 am
In the past several weeks, the United States Food and Drug Administration (“FDA”) granted emergency-use authorization to the Pfizer and Moderna COVID-19 vaccines, prompting employers to ask whether they may require employees to be vaccinated. [read post]
6 Apr 2012, 12:49 pm
Food and Drug Administration, the U.S. [read post]
