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4 May 2014, 10:01 pm by News Desk
Food and Drug Administration released a strategy document on May 2 outlining the agency’s guiding principles for implementing the Food Safety Modernization Act (FSMA). [read post]
9 Jan 2024, 9:05 pm by Coral Beach
As of Jan. 8, the Food and Drug Administration has received 87 confirmed complaints in the outbreak, up from 82 on Dec. 26. [read post]
8 Dec 2021, 9:04 pm by Coral Beach
The patient count in an outbreak of Salmonella infections has more than doubled since first being announced, according to the Food and Drug Administration. [read post]
2 Mar 2023, 12:43 pm by Jonan Pilet
Food and Drug Administration and state health departments of Georgia and Alabama are investigating a Salmonella outbreak associated with the consumption of raw oysters harvested from shellfish harvesting area FL-3012 in Cedar Key, FL. [read post]
22 Jan 2013, 4:17 pm by Lebowitz & Mzhen
Food and Drug Administration (FDA), the CDRH is responsible for medical device safety and quality. [read post]
12 Feb 2013, 7:12 am by Bill Marler
Food and Drug Administration (FDA) is announcing two additional public meetings on the Food Safety Modernization Act (FSMA): Proposed Rules for Produce Safety and for the Preventive Controls for Human Food. [read post]
16 Jun 2015, 10:02 pm by Susan Mayne
Food and Drug Administration, was originally posted here on June 15, 2015.) [read post]
2 Jul 2014, 10:03 pm by Lydia Zuraw
Food and Drug Administration asking that dairy farms be exempted from the intentional adulteration rule of the Food Safety Modernization Act (FSMA). [read post]
30 Aug 2023, 9:03 pm by News Desk
Food and Drug Administration and other organizations provide crucial guidelines for residents to safeguard their food and health. [read post]
2 Jul 2022, 8:53 am by Jonathan Rosenfeld
The Food and Drug Administration issued a warning against the prolonged usage of Zantac and other drugs in its class after a study found they could cause birth defects, including heart problems. [read post]
16 Jun 2016, 2:46 pm by Dr. Shezad Malik
The Food and Drug Administration (FDA) issued a drug safety communication stating that it has revised the warning labels of SGLT2 inhibitors, including Invokana, to include information about acute kidney injury. [read post]
9 Jan 2012, 6:35 pm by Zachary Spilman
Reuters has the story: The Food and Drug Administration is warning patients about a potential mix-up between powerful prescription pain drugs and common over-the-counter medications like Excedrin and Gas-X made at a Novartis manufacturing plant. [read post]
20 Mar 2010, 5:26 pm by Larry Jones
The Federal Food and Drug Administration notified healthcare professionals and patients that, based on review of data from a large clinical trial and other sources, there is an increased risk of muscle injury in patients taking the highest approved dose of the cholesterol-lowering medication, Zocor (simvastatin) 80 mg, compared to patients taking lower doses of simvastatin and possibly other drugs in the "statin" class. [read post]
15 Mar 2012, 3:07 am by Robert Kraft
They are proposing a bill to be added to an important, bill regarding the Food and Drug Administration. [read post]
2 Jul 2022, 8:53 am by Jonathan Rosenfeld
The Food and Drug Administration issued a warning against the prolonged usage of Zantac and other drugs in its class after a study found they could cause birth defects, including heart problems. [read post]
31 Jul 2009, 7:25 am
The Food and Drug Administration gains significant new authority to regulate all aspects of food and how it gets to American tables under the measure. [read post]
18 Jun 2010, 10:00 am by Lucas A. Ferrara, Esq.
Letter to Tobacco Manufacturers on Tobacco Products Labeled or Advertised with the Descriptors "Light," "Low," "Mild," or Similar Descriptors Food and Drug Administration Center for Tobacco Products 9200 Corporate Boulevard Rockville MD 20850-3229 June 17, 2010 Dear Tobacco Manufacturer: The Food and Drug Administration (FDA) is providing this notice to remind manufacturers, including importers of finished… [read post]
6 May 2010, 7:10 am by Carey, Danis & Lowe
Food and Drug Administration has issued a warning to Teva Pharmaceutical Industries Ltd.'s Parenteral Medicines unit about manufacturing problems that contaminated an anesthetic. [read post]
4 May 2009, 6:00 am
You can see an Associated Press video of the recall here: "The Food and Drug Administration said the company that makes the dietary supplement has agreed to recall 14 Hydroxycut products. [read post]