Genetic testing company 23andMe is facing a class action lawsuit alleging that the Silicon Valley startup misled customers with advertising for its personalized DNA test kit.
The Food and Drug Administration has ordered Google-backed genetic test maker 23andMe to halt sales of its personalized DNA test kits, saying the company has failed to show that the technology is supported by science.
Heart-clogging trans fats were once a staple of the American diet, plentiful in baked goods, microwave popcorn and fried foods. Now, mindful of the health risks, the Food and Drug Administration is getting rid of what’s left of them for good.
About 12 percent of spices brought into the U.S. are contaminated with dirt, insect parts, rodent hairs and other filth, according to an FDA Draft report. In addition, the report found spices were twice as likely as other inspected foods to be contaminated with salmonella. More than 80 different types of salmonella were detected.
The Food and Drug Administration is trying to solve a stubborn mystery surrounding the deaths of almost 600 dogs that ate jerky treats, and officials are hoping pet owners and veterinarians can help them figure out what exactly may be causing the illnesses.
The F.D.A. has been looking into scores of complaints from dog owners who say their animals got sick after eating Beneful dog food. The agency said, while it generally does not comment on an open investigation, it has seen a spike in complaints since January after several media reports about the dog food.
Gilead Sciences said Monday that the Food and Drug Administration rejected two marketing applications for HIV treatments, citing quality control problems at the Foster Citry company’s manufacturing facilities.
As the Food and Drug administration is expected to approve the sale of genetically-modified salmon, Trader Joe’s and Whole Foods Market said they won’t sell the fish.
A Berkeley-based company is recalling frozen pizzas that may contain metal fragments.
The Food and Drug Administration is requiring makers of Ambien and similar sleeping pills to lower the dosage of their drugs, based on studies suggesting patients face a higher risk of injury due to morning drowsiness.