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FDA Recalls RegenErect

On February 24, 2012 the Food and Drug Administration (FDA) announced a nationwide recall of RegenErect, which was produced by Regeneca, Inc., previously known at Ethos Environmental, Inc. This product was marketed as a male enhancement pill. According to the company, RegenErect contains Tadalafil, which is an approved drug to treat male Erectile Dysfunction (ED). Unlike Tadalafil, RegenErect has been distributed over the internet and given as samples at public events in the United States and in Puerto Rico.

This drug may lower blood pressure to dangerous levels. Anyone taking nitrates, which are found in some prescription drugs to treat heart disease, diabetes, high cholesterol, and high blood pressure, is at high risk. Men with any of these conditions often experience Erectile Dysfunction and as a result seek products to increase sexual performance.

It is advised that anyone who has purchased RegenErect with the affected lot numbers should return the product for a full refund or exchange. Consumers who have experienced problems as a result of using this pill should also contact their health care provider or physician.

If you or someone you know has been harmed by a recalled medication, contact the attorneys at Abraham, Watkins, Nichols, Sorrels, Agosto & Friend by calling 713-222-7211 or 1-800-870-9584.

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