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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 ...
AN urgent warning has been issued for a common inhaler used by asthma sufferers due to a mistake on the labelling. The error ...
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