Today, the U.S. Food and Drug Administration (FDA) has received 92 reports citing illnesses, hospitalizations and deaths following the consumption of a product called 5-Hour Energy since 2009, including more than 30 reports involving serious or...
Campaign Looks for Whistleblowers Aware of Medical Device and Pharmaceutical Defects
A news release from the Corporate Whistle Blower Center announces a national initiative being launched to look for whistleblowers aware of defective medical devices and pharmaceuticals. This effort is...
FDA Asks Manufacturer to Pull Generic Antidepressant
The Washington Post has noted that concerns regarding the use of generic drugs could again be raised with the revelation that the U.S. Food and Drug Administration (FDA) mistakenly approved a...