Gadget Island recalls 58,000 mg DYNAMITE SUPER capsules due to unapproved drug ingredients. FDA found undeclared sildenafil and tadalafil, making it an illegal product.
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 58,000 mg DYNAMITE SUPER capsules because they contain undeclared sildenafil and tadalafil, which are approved drugs for male sexual enhancement. This makes the product an unapproved drug that could cause health risks.
The capsules contain undeclared sildenafil and tadalafil, which are FDA-approved drugs for male sexual enhancement. These ingredients are not approved for use in this product, making it an unapproved drug that could cause health risks.
Anyone who owns or uses the DYNAMITE SUPER capsules. People most at risk are those who have taken the capsules without knowing they contain unapproved drugs.
Look for the DYNAMITE SUPER capsules with 58,000 mg, 1-count blister card, made in America, UPC 6 75799 37602 7. The lot number is OMS760-B with an expiration date of 12/2025.
Immediately stop using the DYNAMITE SUPER capsules as they contain unapproved drugs that could cause health risks.
FDA analysis found the product contains undeclared sildenafil and tadalafil, which are approved drugs for male sexual enhancement, making it an unapproved drug.
The product is DYNAMITE SUPER capsules, 58,000 mg, 1-count blister card. 58,000 units are recalled.
Check for the DYNAMITE SUPER capsules with 58,000 mg, 1-count blister card, made in America, UPC 6 75799 37602 7, and lot number OMS760-B with expiration 12/2025.
We’ve drafted a message you can send Gadget Island to request your refund or repair — edit it as you like.
Subject: Recall D-0573-2023 — Gadget Island Gadget Island Hello, I own a Gadget Island that is covered by recall D-0573-2023 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.
