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The US FDA informs consumers that Vicerex and Black Ant capsules are recalled because they contain undeclared ingredients: Vicerex contains undeclared tadalafil and Black Ant contains undeclared sildenafil that may pose a threat to consumers. Background of Vicerex and Black Ant Capsules Vicerex and Black Ant, by American Lifestyle, are sold without medical prescription and [...]

The US FDA informs consumers, patients and health professionals that Eba multivitamin supplement is recalled because it might contain undeclared milk components that can cause serious or life-threatening allergic reaction to people with sensitivity to milk. Background of Eba Multivitamin Supplement Eba Multivitamin Supplement, by Saratoga Therapeutics LLC, was distributed nationwide and abroad by internet [...]

Emergency medical personnel and consumers have been informed by the FDA that Lifepak 15 Monitor/Defibrillator by Physio-Control Inc. has been recalled because the device might power off unexpectedly with serious health consequences. Background of Lifepak 15 Monitor/Defibrillator The Lifepak 15 monitor/defibrillator, by Physio-Control Inc., is used to monitor patient heart rhythms and to treat patients [...]

The FDA has informed Emergency Medicine professionals and consumers that the Agency was aware of suspected counterfeit C-A-T tourniquets that may lead to excessive blood loss posing a threat to the victim’s life. Background of Combat Application Tourniquets (C-A-T) The Combat Application Tourniquet (C-A-T) consists of a strap that is placed around an injured limb [...]