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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Pro Power Knight, NUX, and Dynamite Male Enhancement Recalled for Undeclared Drugs

Agency Publication Date: May 4, 2023
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Summary

Gadget Island, Inc. is recalling 786 units of Pro Power Knight Plus, NUX Male Enhancement, and DYNAMITE SUPER capsules because they were found to be tainted with undeclared sildenafil and tadalafil. These ingredients are found in FDA-approved prescription drugs (such as Viagra and Cialis) for the treatment of male sexual enhancement, making these products unapproved drugs. The recall affects 1-count blister cards distributed nationwide in the USA.

Risk

The undeclared ingredients, sildenafil and tadalafil, can interact with nitrates found in some prescription drugs like nitroglycerin, potentially lowering blood pressure to dangerous or life-threatening levels. This is especially concerning for individuals with diabetes, high blood pressure, or heart disease.

What You Should Do

  1. This recall affects Pro Power Knight Plus (2550mg), NUX Male Enhancement, and DYNAMITE SUPER (58,000 MG) capsules sold in single-count blister cards.
  2. Check your packaging for identifying codes: Pro Power Knight Plus UPC 494922905220 (Exp 06/2026), NUX Male Enhancement UPC 601577512363 (Lot RO 927996, Exp 12/25/2024), or DYNAMITE SUPER UPC 675799376027 (Lot OMS760-B, Exp 12/2025).
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Pro Power Knight Plus capsule (2550mg)by Pro Power Knight Plus
Variants: 1-count blister card, 2550mg
UPC Codes:
494922905220
Lot Numbers:
No lot number (Exp 06/2026)

Distributed by Beyond Health and youth Inc, Seattle, WA 98110

Product: NUX Male Enhancement capsuleby NUX
Variants: 1-count blister card
UPC Codes:
601577512363
Lot Numbers:
RO 927996 (Exp 12/25/2024)

Distributed by SX Power CO., Chicago, Il 60612

Product: DYNAMITE SUPER capsule (58,000 MG)by DYNAMITE SUPER
Variants: 1-count blister card, 58,000 MG
UPC Codes:
675799376027
Lot Numbers:
OMS760-B (Exp 12/2025)

Made in America

Product Images

Front of Pro Power Knight Plus Capsule, 2550 mg

Front of Pro Power Knight Plus Capsule, 2550 mg

Back of Pro Power Knight Plus Capsule, 2550 mg

Back of Pro Power Knight Plus Capsule, 2550 mg

Front of NUX Male Enhancement Capsule

Front of NUX Male Enhancement Capsule

Back of NUX Male Enhancement Capsule

Back of NUX Male Enhancement Capsule

Front of DYNAMITE SUPER Capsule 58,000 mg

Front of DYNAMITE SUPER Capsule 58,000 mg

Back of DYNAMITE SUPER Capsule 58,000 mg

Back of DYNAMITE SUPER Capsule 58,000 mg

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92203
Status: Active
Manufacturer: Gadget Island, Inc
Sold By: Beyond Health and youth Inc; SX Power CO.
Manufactured In: United States
Units Affected: 3 products (628 blister cards; 18 blister cards; 140 blister packs)
Distributed To: Nationwide
Agency Last Updated: May 11, 2023

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท FDA Press Release ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.