Aspire36

The U.S. Food and Drug Administartion announced today a recall of supplement products sold under the name Aspire36 and Aspire Lite. The manufacturer, Palo Alto Labs, is recalling the recalled supplements because lab analysis by the FDA of Aspire36 and Aspire Lite samples found the products contained Aildenafil in trace amounts and Dimethyl sildenafil thione (sulfoaildenafil), a purported analog of Sildenafil – an FDA-approved drug used as treatment for male Erectile Dysfunction (ED).