U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS), and Centers for Disease Control and Prevention ...

The recall has been given a Class II classification, indicating there is a significant level of risk posed to consumers in ...

The Food and Drug Administration has identified a Class I recall of Edwards Lifesciences OptiSite Arterial Perfusion Cannula devices due to the potential for serious injury or death.

The FDA today issued a notice warning of a recall of arterial perfusion cannula devices made by Edwards Lifesciences (NYSE:EW ...

Lupin Pharmaceuticals’ Clomipramine Hydrochloride capsules are used “for the treatment of obsessions and compulsions in ...