A&H Focal Recalls 21 Male Enhancement Supplements Due to Presence of Undeclared Erectile Dysfunction Ingredients

Consumers with diabetes, high blood pressure, high cholesterol, or heart disease should avoid the affected products

A&H Focal Recalls 21 Male Enhancement Supplements Due to Presence of Undeclared Erectile Dysfunction Ingredients
March 13, 2017

A&H Focal is recalling a variety of products because many of these products have been historically tested by the U.S. Food & Drug Administration (FDA) and found to contain PDE-5 Inhibitors (i.e. sildenafil, tadalafil, vardenafil, etc.). PDE-5 Inhibitors are the active ingredient in an FDA-approved drug for erectile dysfunction (ED) making these tainted dietary supplements unapproved drugs.

These undeclared active ingredients poses a threat to consumers because the PDE-5 Inhibitors may interact with nitrates found in some prescription drugs such as nitroglycerin and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates.

These products were marketed as dietary supplements for male sexual enhancement. All lots of the listed products sold by A&H Focal since January 2014 to present are included in this recall. The products were mainly sold through Asian Markets located in New Jersey and New York.

Consumers who have any of the above mentioned products should immediately stop consumption and properly discard it.

Consumers with any additional questions or concerns regarding this recall can contact Mr. Henry Choo at (646) 327-8522.