Beamonstar Products recalls Velextra All-Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 & 12 capsule bottles, Manufact
Recalled September 11, 2013 · FDA recall D-930-2013 · Beamonstar Products
Hazard
Marketed Without an Approved NDA/ANDA; products have been found to contain tadalafil, the active ingredient in an FDA approved product used to treat erectile dysfunction, making this product an unapproved drug · FDA Class I
Units
145,632 capsules
Sold at
US states nationwide and international.
Description
Marketed Without an Approved NDA/ANDA; products have been found to contain tadalafil, the active ingredient in an FDA approved product used to treat erectile dysfunction, making this product an unapproved drug
Product
Velextra All-Natural Herbal Supplement, packaged in 1 & 2 capsule blister packs and 4, 10 & 12 capsule bottles, Manufactured For: BeaMonstar Products Queen Creek, AZ
Manufacturer(s)
Beamonstar Products
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →