Search for: "U.S. Food and Drug Administration"
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12 Dec 2013, 10:01 pm
Food and Drug Administration (FDA) is one step closer to implementing FSMA. [read post]
1 Sep 2021, 12:45 pm
Food and Drug Administration (FDA) review of a large randomized safety clinical trial, we have concluded there is an increased risk of serious heart-related events such as heart attack or stroke, cancer, blood clots, and death with the arthritis and ulcerative colitis medicines Xeljanz and Xeljanz XR (tofacitinib). [read post]
31 Dec 2007, 12:46 am
Food and Drug Administration said on Wednesday.The test strips are used by diabetic patients to monitor their daily blood sugar levels.Bayer Diabetes Care said the recalled test strips were produced on new manufacturing equipment and that it has fixed the problem.Some 53 production lots were affected by the recall, totaling 230,000 bottles of strips, a Bayer spokeswoman said. [read post]
8 Dec 2011, 6:44 am
Food and Drug Administration (FDA) recently announced a recall of certain 8-ounce Almond Clusters because they may contain peanuts. [read post]
8 Dec 2011, 12:15 pm
Food and Drug Administration issued a voluntary recall of certain one half pound packaged cheeses and cheese gift boxes sold between September 30, 2011 and December 3, 2011. [read post]
26 Nov 2021, 6:34 am
Food and Drug Administration’s (FDA) guidelines for selling e-cigarette products, which required all manufacturers to file paperwork known as premarket tobacco product applications (PMTAs) by Sept. 9, 2020. [read post]
8 Dec 2011, 6:44 am
Food and Drug Administration (FDA) recently announced a recall of certain 8-ounce Almond Clusters because they may contain peanuts. [read post]
8 Dec 2011, 12:15 pm
Food and Drug Administration issued a voluntary recall of certain one half pound packaged cheeses and cheese gift boxes sold between September 30, 2011 and December 3, 2011. [read post]
20 Jul 2011, 2:57 pm
Food and Drug Administration (FDA) warned people not to drink unpasteurized milk from South Carolina-based Tucker Adkins Dairy because it may be contaminated with Campylobacter. [read post]
10 Jun 2025, 7:43 pm
Food and Drug Administration (FDA) classified the recall as a Class I event—the agency’s most serious category—indicating that the issues could potentially lead to serious injury or death. [read post]
10 Nov 2007, 1:08 pm
Bourne, Special Agent in Charge, Food and Drug Administration, Office of Criminal Investigations, and Lee Huttenbach, Special Agent in Charge, U.S. [read post]
31 Dec 2016, 7:06 am
Food and Drug Administration (“FDA”) surprised many in the radiopharmacy industry by issuing a long-awaited draft guidance entitled “Compounding and Repackaging of Radiopharmaceuticals by State-Licensed Nuclear Pharmacies. [read post]
22 Jan 2016, 10:01 pm
Food and Drug Administration from the cheeses manufactured by Roos Foods. [read post]
31 Aug 2014, 9:06 am
Food and Drug Administration (FDA) fast-tracked its approval and allowed it to hit the market after only a single large clinical trial. [read post]
3 Jun 2014, 11:38 am
Food and Drug Administration (FDA) made available data on millions of reports of drug adverse events and medication errors made to FDA between 2004 and 2013. [read post]
3 Aug 2011, 2:59 am
Four years after the Food and Drug Administration proposed guidelines for gluten-free labeling, the issue of what qualifies as "gluten-free" is back on the table.Today the agency is reopening the comment period for its rules on gluten-free labeling, which were drafted in 2007 but have not yet been adopted. [read post]
5 Mar 2010, 4:57 pm
As part of the Salmonella Montevideo investigation, the Food and Drug Administration has been actively investigating the supply chain of black and red pepper supplied to Daniele International Inc., Pascoag, R.I. [read post]
5 Mar 2023, 9:03 pm
Food and Drug Administration and the U.S. [read post]
23 Apr 2015, 3:41 pm
The guidance arises from the 2012 Food and Drug Administration Safety and Innovation Act § 1123, amending Food, Drug & Cosmetic Act § 569B, which codified FDA’s longstanding practice of accepting scientifically-valid clinical data obtained from foreign clinical studies in support of premarket submissions for devices. [read post]
23 Apr 2015, 3:41 pm
The guidance arises from the 2012 Food and Drug Administration Safety and Innovation Act § 1123, amending Food, Drug & Cosmetic Act § 569B, which codified FDA’s longstanding practice of accepting scientifically-valid clinical data obtained from foreign clinical studies in support of premarket submissions for devices. [read post]
