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18 Jun 2009, 2:04 pm
., and four of its executives were indicted Tuesday on federal charges that they improperly promoted a bone filler for purposes not approved by the Food and Drug Administration including encouraging its use in what prosecutors called ‘unauthorized' human trials. [read post]
20 Mar 2020, 9:32 am
Food and Drug Administration (“FDA”) and the Federal Trade Commission (“FTC”) issued warning letters to seven companies allegedly selling unapproved products that may violate federal law by making deceptive or scientifically unsupported claims about their ability to treat coronavirus (COVID-19). [read post]
4 Jan 2009, 9:50 pm
Food and Drug Administration (FDA).The company has identified a condition in the manufacturing equipment that has since been corrected. [read post]
14 Jan 2010, 3:27 pm
The only problem, says the Food and Drug Administration, is there is no scientific evidence to back up the claims made by the e-cigarette manufacturers, distributors and marketers. [read post]
20 Jul 2010, 1:39 am
In 2005, the Food and Drug Administration (FDA) warned doctors about a study showing that babies born to women who took Paxil during the first trimester of pregnancy had a higher rate of major birth defects. [read post]
31 Jan 2023, 1:19 pm
Food and Drug Administration (FDA) recently proposed “a change from time-based deferrals to assessing blood donor eligibility using gender-inclusive, individual risk-based questions to reduce the risk of transfusion-transmitted HIV. [read post]
20 Jan 2017, 1:52 pm
Last week the US Food and Drug Administration (“FDA”) provided guidance on the Nonproprietary Naming of Biological Products. [read post]
9 Aug 2019, 8:58 am
CHICAGO (August 9, 2019) – The US Food and Drug Administration has received at least 127 reports of seizures or other neurological symptoms possibly related to e-cigarettes, the agency announced this week. [read post]
14 Aug 2008, 4:34 am
The Food and Drug Administration (FDA) issued a warning last month to doctors who treat patients with electronic devices such as pacemakers, cardiac defibrillators and insulin pumps. [read post]
17 Jun 2009, 1:01 am
Food and Drug Administration (FDA). [read post]
2 Oct 2008, 9:37 pm
Medtronic and the Food and Drug Administration (FDA) issued a Class I Recall of the Medtronic Neuromodulation INDURA IP. [read post]
29 May 2019, 7:12 am
Reuters reports that the US Food and Drug Administration is beginning to tighten regulations on over-the-counter sunscreen. [read post]
3 Jun 2012, 6:31 pm
Food and Drug Administration is warning consumers that Reumofan Plus, marketed as a “natural” dietary supplement for pain relief and other serious conditions, contains several active pharmaceutical ingredients not listed on the label that could be harmful.Consumers who are currently taking Reumofan Plus or who have recently stopped taking Reumofan Plus should immediately consult a health care professional. [read post]
1 May 2012, 11:16 am
Gibson, Dunn & Crutcher's health care practice in Washington will get a boost with the addition of a new attorney from the Food and Drug Administration's Office of Chief Counsel. [read post]
16 Jul 2021, 11:27 am
Food and Drug Administration (FDA) yesterday to ban per- and poly-fluoroalkyl substances (PFAS) from food contact uses, and to “take aggressive action to protect consumers from all PFCs [per- and poly-fluorinated compounds]. [read post]
18 Apr 2016, 10:00 pm
Food and Drug Administration (FDA) to issue an import alert yesterday on Malaysian shrimp and prawns. [read post]
1 Feb 2011, 1:59 am
""It is noteworthy that the government's previous recommendation that consumers eat five to seven ounces from the meat, poultry and beans group will remain unchanged, said the group's executive vice president, James Hodges, adding that the meat, poultry, fish, eggs, nuts food group is the only group that Americans consume in the recommended amount.The seafood industry seized on the new guidelines to urge the Food and Drug Administration to… [read post]
29 Apr 2019, 9:01 pm
That meeting on Feb. 26, which included FSIS Administrator Carmen Rottenberg, was about food products derived from cells of livestock and poultry. [read post]
Los Angeles Dangerous Drug Trial: Man Claims Motrin Caused Him to Develop Toxic Epidermal Necrolysis
23 Aug 2011, 2:19 pm
He also claims that the drug manufacturer misrepresented the results of the study to the Food and Drug Administration and wasn't entirely truthful about the risk of SJS when it said the drug could be sold without a prescription. [read post]
2 Jan 2014, 10:01 pm
Food and Drug Administration (FDA) advising that it intends to petition the agency to allow foods containing GMOs to be labeled as “natural. [read post]
