Gadget Island, Inc recalls NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
Recalled May 10, 2023 · FDA recall D-0572-2023 · 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
18 blister cards
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
NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
Manufacturer(s)
Gadget Island, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →