Gadget Island, Inc recalls DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.
Recalled May 10, 2023 · FDA recall D-0573-2023 · Gadget Island
Hazard
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug. · FDA Class I
Units
140 blister packs
Sold at
Nationwide in the USA.
Description
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Product
DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.
Manufacturer(s)
Gadget Island, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →