This product is currently being sold as a dietary supplement throughout the U.S. Good Health, Inc. is conducting a voluntary recall after being informed by the Food and Drug Administration (FDA) that a lab analyses found that the product tested from certain batches of Vialipro contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED) making this product an unapproved drug. The active drug ingredient is not listed on the product label. The undeclared ingredient may pose a threat to the consumer because the interaction of the analogue with some prescription drugs (such as nitroglycerin) may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take other prescription drugs. Erectile Dysfunction is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance.

Vialipro Sold Under the Following Lot Numbers
Lot Number
80409 Capsules, 10 Count All Dates
80661 Capsules, 10 Count All Dates
 81146 Capsules, 10 Count All Dates
90132 Capsules, 10 Count All Dates
90265 Capsules, 10 Count All Dates
90587 Capsules, 10 Count All Dates
90826 Capsules, 10 Count All Dates
91065 Capsules, 10 Count All Dates
00197 Capsules, 10 Count All Dates
'00347 Capsules, 10 Count All Dates

Recommendation:
Health authority Abu Dhabi advises consumers not to purchase this product via the internet; if the product was purchased locally you are advised not to use it and to return it back to the vendor.

For more information, please follow the link
http://www.fda.gov/Safety/Recalls/ucm219558.htm