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10 Feb 2009, 1:28 pm
According to the Food and Drug Administration and a recent New York Times story, many popular weight loss supplements contain the drugs Sibutramine, Rimonabant, Phenolphthalein, and Bumetanide. [read post]
13 Aug 2010, 2:59 am
Food and Drug Administration to the Goshen, CA-based Western Milling Company for a comprehensive inspection last March 18-31.Western Milling, a unit of O.H. [read post]
26 Aug 2010, 2:59 am
Food and Drug Administration said in an Aug. 13 warning letter to the company.FDA said inspectors found "serious deviations from low-acid food regulations" at the manufacturing facility owned by Amish Wedding Foods Inc. located in Millersburg.The warning letter followed inspections at Amish Foods conducted last April and May. [read post]
28 Jul 2014, 10:02 pm
Food and Drug Administration Commissioner Margaret Hamburg on Monday to ask for more information regarding the agency’s efforts to curb the overuse of antibiotics in food animal production. [read post]
10 Apr 2016, 12:03 pm
Food and Drug Administration for approving the first ever genetically engineered animal for human consumption, a salmon engineered to grow quickly. [read post]
13 Dec 2023, 9:30 pm
Food and Drug Administration, Frohlich describes the emergence of our present information age in food and diet markets and examines how powerful government offices inform the public about what they consume. [read post]
22 Nov 2010, 7:48 am
The injectable form of pentobarbital is made by Wyeth Ayerst, according to the Food And Drug Administration; Wyeth is a unit of Pfizer Inc. [read post]
14 Apr 2011, 7:01 am
Food and Drug Administration issued a safety warning April 7 about a link between benzocaine and a condition called methemoglobinemia. [read post]
4 Dec 2016, 10:00 pm
Drug Administration’s Cincinnati district office notified the company’s president and owner, David Bernstein, of the action switching the Landing’s Galley catering operation from “approved” to “provisional” in a Nov. 23 warning letter made public in recent days. [read post]
9 Dec 2011, 1:59 am
Food and Drug Administration has agreed to decide by March 31, 2012 whether bisphenol A, the controversial chemical known as BPA, should be banned from use in food and beverage packaging.The FDA agreed to the deadline as part of the settlement of a lawsuit filed by the Natural Resources Defense Council (NRDC), one of many consumer and environmental groups that advocate banning BPA in food packaging.Three years ago, the NRDC petitioned the FDA to ban the… [read post]
21 May 2013, 10:02 pm
Food and Drug Administration over the agency’s delayed food safety rules continued last week as a judge ruled that FDA had more time to come up with a schedule for releasing the outstanding rules. [read post]
25 Jun 2009, 12:33 pm
The Food and Drug Administration (FDA) has warned consumers not to eat two brands of pistachios repacked by Orca Distribution West Inc. of Anaheim, California. [read post]
29 Sep 2015, 2:56 pm
Food and Drug Administration (FDA) are investigating a multistate outbreak of Salmonella Poona infections. 671 people infected with the outbreak strains of Salmonella Poona have been reported from 34 states, an increase of 113 cases since the last update on September 22. [read post]
15 Nov 2014, 10:30 am
The Philippines Food and Drug Administration (FDA) has announced the recall of several batches of Arrowhead Mills Peanut Butter products over possible contamination from Salmonella. [read post]
19 Jul 2012, 5:51 pm
The Food and Drug Administration (FDA) placed Lexapro (escitalopram) in Category C because the federal health agency was concerned this common prescribed antidepressant medication might have the capacity to harm developing children. [read post]
11 Oct 2011, 12:00 am
The Food and Drug Administration's Center for Devices and Radiological Health (CDRH) announced last week that it is creating a “Network of Experts” to give the agency rapid access to information and advice about emerging medical technologies. [read post]
11 May 2012, 5:00 pm
The federal government’s Food and Drug Administration (FDA) recently issued an updated warning that encouraged medical professionals to report adverse events related to Zoloft ingestion during pregnancy to the FDA’s MedWatch Program. [read post]
14 Sep 2010, 3:15 pm
Symbiq One- and Two-Channel Infusers manufactured by Hospira are subject to a class 1 US Food and Drug Administration (FDA) recall because of a potential for the failure to detect air in the line at the end of an infusion. [read post]
27 Feb 2012, 9:22 am
The Food and Drug Administration (FDA), the federal agency responsible for protecting Americans from harmful medical devices, has issued repeated warnings about the risks of transvaginal mesh devices. [read post]
30 Jan 2012, 5:39 pm
According to estimates by the Food and Drug Administration, more than 300,000 women every year undergo transvaginal mesh procedures designed to treat their pelvic organ prolapse (POP) and stress urinary incontinence (SUI). [read post]
