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15 Jun 2016, 8:45 am
Food and Drug Administration advises consumers with severe peanut allergies to avoid the recalled products because of peanut residue in the flour used to make the products. [read post]
14 Jun 2016, 9:14 am
Food and Drug Administration has stated that the amount of peanut exposure from the flour is low and not expected to cause adverse health effects in the vast majority of peanut allergic consumers. [read post]
21 Jul 2009, 8:12 am
Food and Drug Administration (FDA) later that year by five major honey producers and processors, asking the federal agency to establish a U.S. standard of identity for honey. [read post]
19 Feb 2009, 12:55 am
The District Court denied defendants' motion to dismiss and granted the plaintiffs' motion for class certification, but shortened the class period by more than one year, finding that investors could not have reasonably relied on defendants' alleged misrepresentations after February 1, 2006, the date the Food and Drug Administration ("FDA") staff published a report on a clinical study of Celebrex, a popular anti-inflammatory medication. [read post]
29 Feb 2012, 11:00 am
Hauser submits that “patients in the United States continue to be exposed to underperforming and potentially hazardous medical devices after they have been approved by the Food and Drug Administration … despite multiple recalls and some tragic adverse events. [read post]
28 Jan 2016, 11:40 am
In the United States, at least 2 million antibiotic-resistant illnesses and 23 000 deaths occur each year, at a cost to the U.S. economy of at least $30 billion (2). [read post]
6 Nov 2019, 1:04 pm
” The Food & Drug Administration (FDA) actually has a database dedicated to medical device recalls, which includes hernia mesh products. [read post]
4 Jun 2016, 11:00 am
Not only was the cutting guide defective, the United States Food and Drug Administration (FDA) specifically told the CEO that they were not approving the cutting guide and that he could not ship it to surgeons. [read post]
27 Feb 2012, 10:09 am
Fort Worth, TX February 27, 2012 Parker McDonald, P.C. recently reported on The New York Times investigation which showed DePuy Orthopaedics, Inc. continued to market one of its hip devices after it was rejected by the Food and Drug Administration. [read post]
7 Jul 2010, 11:00 am
Food and Drug Administration announced it has approved the Implantable Miniature Telescope (IMT) to improve vision in some patients with end-stage age-related macular degeneration (AMD). [read post]
3 Jun 2014, 1:05 pm
Food and Drug Administration (“FDA”) began notifying manufacturers of reports of complications linked to the devices. [read post]
20 Dec 2016, 5:00 am
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
7 Feb 2017, 8:00 am
The United States Food and Drug Administration (FDA) has begun to investigate this issue and has found that on average, 18 explosions occur each year, and some of these explosions result in serious personal injury. [read post]
8 Sep 2011, 9:51 pm
Johnson & Johnson (JNJ) and rival makers of transvaginal meshes told Food and Drug Administration advisers they agreed on the need for more safety studies of the implants as well as labeling changes to warn of potential risks. [read post]
24 Oct 2014, 6:08 am
Food and Drug Administration required device makers to submit new versions of the artificial hips for pre-market approval. [read post]
21 Jun 2010, 8:07 am
Food and Drug Administration has taken notice of the issue and claims to have several safety steps in the works, including the possibility of having device makers print the radiation dose on x-rays and images so doctors and patients are more aware of the exposure. [read post]
15 Jun 2012, 3:52 pm
In 2008, the United States Food and Drug Administration (“FDA”) issued a Public Health Notification (“PHN”) to warn patients about adverse effects related to urogynecologic use of surgical mesh. [read post]
6 Oct 2014, 4:29 pm
Food and Drug Administration said vaginal-mesh inserts should be subject to stricter safety requirements because they are high-risk devices. [read post]
20 Dec 2016, 5:00 am
They may be promoted by a government oversight agency, such as the Food and Drug Administration (FDA) or the Consumer Product Safety Commission (CPSC). [read post]
20 Feb 2017, 12:28 pm
According to the Food and Drug Administration, as of 2012, about 324,200 people worldwide have received cochlear implants, and more than 26 percent of recipients lived in the United States. [read post]
