The U.S. Food and Drug Administration (FDA) recently required manufacturers of cholesterol-lowering statin drugs to place warning labels on their products so consumers and doctors are aware of the increase of developing adult-onset diabetes, also...
Class I Recall Issued on Medtronic Inc. Guidewires Used in Heart Procedures
Most product recalls are categorized by the U.S. Food and Drug Administration (FDA) as Class I, II or III. The most serious is a Class I recall, in which there is reasonable probability that in using the product it will cause serious injury or...
Clomid Birth Defect Risk
Watch on YouTube.