Viapro herbal supplement is recalled

Washington -- The U.S. Food and Drug Administration announced a nationwide recall of Viapro herbal supplements because of a potential health hazard.

EG Labs LLC of New York initiated the voluntary recall of all lots of Viapro in 375 mg capsules after the FDA found the product contained thiomethisosildenafil, a potentially harmful undeclared ingredient, The FDA said the chemical is an analog of sildenafil, the active ingredient of a FDA-approved drug used to treat erectile dysfunction.

"The use of undeclared chemicals pose a threat to consumers because they may harmfully interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels," the FDA said, noting people with diabetes, high blood pressure, high cholesterol or heart disease often take such nitrates.

The recalled Viapro capsules were sold nationwide as an aid to improving sexual performance. The product was available in 2-capsule blisters, 1 capsule blisters and 10 capsule bottles.

The company said customers can receive a refund by returning the product to: Seaboard Tampa Terminal, 6708 Harney Road, Tampa Fla., 33610.

Copyright 2008 by United Press International.