Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

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.

© 2026 Go Backs. All rights reserved.

Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Ummzy, LLC: Sexual Enhancement Capsules Recalled for Undeclared Drug Ingredients

Agency Publication Date: July 16, 2021
Share:
Sign in to monitor this recall

Summary

Ummzy, LLC is recalling Krazy Night, Shogun-X, and Thumbs up 7 Red 70K capsules because they contain undeclared sildenafil, tadalafil, and vardenafil. Approximately 527 units were affected across the three brands. These products were marketed as dietary supplements, but the presence of prescription drug ingredients makes them unapproved drugs that have not been evaluated for safety or effectiveness. Consumers should immediately stop using these products and contact their healthcare provider or pharmacist for guidance.

Risk

The undeclared ingredients sildenafil, tadalafil, and vardenafil are phosphodiesterase (PDE-5) inhibitors used for erectile dysfunction which can interact with nitrates found in some prescription drugs (such as nitroglycerin), potentially lowering blood pressure to dangerous levels. This poses a significant health risk to consumers with diabetes, high blood pressure, high cholesterol, or heart disease who often take nitrates.

What You Should Do

  1. Identify if you have the affected products by checking for these details: Krazy Night capsules in 1-count blisters or 10-count boxes (UPC 746695241860); Shogun-X capsules in 10-count boxes (UPC 118122030185); or Thumbs up 7 Red 70K capsules in 10-count boxes (UPC 617135894680).
  2. Check the expiry dates on your packaging; all lots within their expiry date are included in this recall.
  3. Immediately stop using any affected capsules and dispose of them or return them to the place of purchase.
  4. Contact your healthcare provider or pharmacist if you have experienced any problems that may be related to taking or using these drug products.
  5. Return any unused product to the place of purchase for a refund and contact Ummzy, LLC for further instructions.
  6. For additional questions or to report a reaction, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Contact healthcare provider or return for refund.

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

Affected Products

Product: Krazy Night capsule (1-count per blister card or 10-count box)
UPC Codes:
746695241860
Lot Numbers:
All lots within expiry
Product: Shogun-X capsules (10-count box)
UPC Codes:
118122030185
Lot Numbers:
All lots within expiry
Product: Thumbs up 7 Red 70K capsules (10-count box)
UPC Codes:
617135894680
Lot Numbers:
All lots within expiry

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 87624
Status: Resolved
Manufacturer: Ummzy, LLC
Sold By: Nationwide retailers
Manufactured In: United States
Units Affected: 2 products (364 boxes/10 capsules per box; 163 boxes/10 capsules per box)
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 · 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.