According to Drug Watch, the U.S. Food and Drug Administration (FDA) is proposing a new safety system to monitor medical devices. The new plan would entail unique device identifications (UDIs) that...
Zithromax Brochure Overstates Benefits and Minimizes Risks
According to a report from SFGate.com, the U.S. Food and Drug Administration (FDA) has issued a warning to drug manufacturer, Pfizer due to its Zithromax brochure overstating the benefits and...
FDA Recalls 3 Dietary Supplements Due to Potential Salmonella
(July 12, 2012)
The U.S. Food and Drug Administration (FDA) notified consumers and healthcare professionals of a recall of three dietary supplements due to potential salmonella...