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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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Medium RiskFDA Drug
Medications & Supplements/Dietary Supplements

Bit & Bet LLC: Thumbs Up 7 Blue 69K Capsules Recalled for Undeclared Drug Ingredients

Agency Publication Date: May 18, 2021
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Summary

Bit & Bet LLC is recalling 3,894 boxes (totaling 38,940 capsules) of Thumbs Up 7 Blue 69K dietary supplements because FDA laboratory analysis found they contain sildenafil and tadalafil. These are active drug ingredients found in FDA-approved prescription drugs like Viagra and Cialis, but they are not listed on the product label. The recall affects all lots of the product that are currently within their expiration dates. Consumers who have purchased these capsules should contact their healthcare provider or pharmacist for guidance and return any unused product to the place of purchase for a refund.

Risk

These undeclared ingredients can interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous or life-threatening levels. This poses a significant risk to people with diabetes, high blood pressure, high cholesterol, or heart disease who often take nitrates.

What You Should Do

  1. Identify the affected product by looking for 'Thumbs Up 7 Blue 69K' in a blue box containing 10 capsules packaged in blister foil sheets.
  2. Check the back of the box for UPC 617135894673 and confirm if the product is still within its expiration date, as all unexpired lots are included in this recall.
  3. Immediately stop using the product if you have it in your possession.
  4. Contact your healthcare provider or pharmacist if you have experienced any problems that may be related to taking this product.
  5. Return any unused capsules to the place of purchase to receive a full refund.
  6. Contact Bit & Bet LLC at their Cliffside Park, New Jersey location for further instructions regarding the return or disposal of the product.
  7. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Manufacturer refund

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

Affected Products

Product: Thumbs Up 7 Blue 69K (10 capsules)
Model:
Recall #: D-0388-2021
UPC Codes:
617135894673
Lot Numbers:
All lots within expiry

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87630
Status: Resolved
Manufacturer: Bit & Bet LLC
Sold By: Ummzy LLC.
Manufactured In: United States
Units Affected: 3894 ten-count boxes (38,940 capsules)
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.