Gadget Island recalls NUX Male Enhancement capsules due to FDA findings of undeclared sildenafil and tadalafil, making them unapproved drugs. Consumers should stop using these products immediately.
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.
Gadget Island is recalling NUX Male Enhancement capsules because they contain undeclared sildenafil and tadalafil, ingredients approved for male sexual enhancement. This makes the product an unapproved drug that could pose health risks.
The capsules contain undeclared sildenafil and tadalafil, which are FDA-approved drugs for male sexual enhancement. Since these products were marketed without proper FDA approval, they could cause serious health issues like adverse reactions or interactions with other medications.
Anyone who purchased the NUX Male Enhancement capsules from the distributed lot (RO 927996) between the product's distribution date and expiration (12/25/2024). Men using these capsules for sexual enhancement are at highest risk.
Check for the product name 'NUX Male Enhancement capsule', 1-count blister card, distributed by SX Power CO. in Chicago, IL. The lot number is RO 927996 with an expiration date of 12/25/2024.
Immediately stop using the NUX Male Enhancement capsules if you have them.
The FDA found that the product contains undeclared sildenafil and tadalafil, which are ingredients approved for male sexual enhancement, but the product was marketed without FDA approval.
Stop using the product immediately and contact the manufacturer for further instructions.
No, this product is not safe to use as it contains undeclared drugs that could cause serious health risks.
We’ve drafted a message you can send Gadget Island to request your refund or repair — edit it as you like.
Subject: Recall D-0572-2023 — Gadget Island Gadget Island Hello, I own a Gadget Island that is covered by recall D-0572-2023 from Gadget Island. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
