FDA-Drug2023-05-10Class I
NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
Gadget Island, Inc
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.
Sold states
Nationwide in the USA.
Affected count
18 blister cards
Manufactured in
1275 Halyard Dr Ste 175, West Sacramento, CA, United States
Products
NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0572-2023Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief