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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

Nuri Trading LLC: Dietary Supplement Capsules Recalled for Undeclared Erectile Dysfunction Drugs

Agency Publication Date: July 19, 2021
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Summary

Nuri Trading LLC is recalling several sexual enhancement supplement capsules, including Shogun-X 7000, Thumbs Up 7 Black 25K, Thumbs Up 7 White 11K, and 69MODE Blue 69. These products were found to contain undeclared prescription drug ingredients, including sildenafil, tadalafil, and vardenafil, which are used to treat erectile dysfunction. These ingredients are not listed on the labels, making the products unapproved drugs with unproven safety and efficacy. Consumers should contact a healthcare provider or pharmacist regarding the use of these products and return any unused portions to the place of purchase for a refund.

Risk

The undeclared ingredients can interact with nitrates found in some prescription medications, such as nitroglycerin, which may cause blood pressure to drop to life-threatening levels. Men with diabetes, high blood pressure, high cholesterol, or heart disease are often prescribed nitrates and are at significant risk of harm from these tainted products.

What You Should Do

  1. Check your supplements to see if you have Shogun-X 7000, Thumbs Up 7 Black 25K, Thumbs Up 7 White 11K, or 69MODE Blue 69 capsules.
  2. Verify if your product is part of the recall by checking the packaging: this affects all lots within their expiration dates sold in 1-count blister cards or 10-count boxes.
  3. Stop using these products immediately as they contain undeclared prescription drugs that may pose serious health risks.
  4. Contact your healthcare provider or pharmacist for guidance if you have taken any of these products, especially if you take medications containing nitrates.
  5. Return any unused product to the place of purchase for a full refund or contact Nuri Trading LLC for further instructions.
  6. Contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

๐Ÿ’ฐFull Refund

Full refund upon return.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Shogun-X 7000 capsule (1-count blister card or 10-count box)
Model:
D-0685-2021
Lot Numbers:
all lots within expiry
Product: Thumbs Up 7 Black 25K capsule (1-count blister card or 10-count box)
Model:
D-0686-2021
Lot Numbers:
all lots within expiry
Product: Thumbs Up 7 White 11K capsule (1-count blister card or 10-count box)
Model:
D-0687-2021
Lot Numbers:
all lots within expiry
Product: 69MODE Blue 69 capsule (10-count box)
Model:
D-0688-2021
Lot Numbers:
all lots within expiry

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87641
Status: Active
Manufacturer: Nuri Trading LLC
Manufactured In: United States
Distributed To: Nationwide

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 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.