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

Natures Rx: Silver Bullet Male Enhancement Capsules Recalled for Undeclared Sildenafil

Agency Publication Date: December 31, 2019
Share:
Sign in to monitor this recall

Summary

Natures Rx is recalling 2,800 units of Silver Bullet (725mg) male enhancement capsules because they were found to contain sildenafil, an undeclared active pharmaceutical ingredient. Sildenafil is the generic version of the prescription drug Viagra, and its presence in a dietary supplement makes the product an unapproved drug. These capsules were sold in 10-count blister foil packages nationwide across the United States. Consumers should stop using this product immediately and consult a healthcare provider, as sildenafil can cause serious health risks when it interacts with other medications.

Risk

The undeclared sildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and can lower blood pressure to dangerous or life-threatening levels. This pose a significant risk to individuals 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 product by checking the packaging for 'Silver Bullet' 10-count male enhancement capsules (725mg per capsule).
  2. Check the back of the blister foil package for Lot number 01251ZX1 with an expiration date of 11/2022 and UPC 610877392698.
  3. Stop using the product immediately if it matches the identified lot number and expiration date.
  4. Contact your healthcare provider or pharmacist for guidance regarding any health concerns or potential drug interactions.
  5. Return any unused product to the place of purchase for a refund and contact Natures Rx for further instructions.
  6. For additional questions or to report a complaint, contact the FDA Consumer Complaint line at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Refund for unused product

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

Affected Products

Product: Silver Bullet Male Enhancement Capsules (725mg, 10-count)
UPC Codes:
610877392698
Lot Numbers:
01251ZX1 (Exp 11/2022)
Date Ranges: 11/2022

Product Images

Silver bullet, 10 male enhancement capsules

Silver bullet, 10 male enhancement capsules

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84279
Status: Resolved
Manufacturer: Natures Rx
Sold By: Silver Bullet Ltd
Manufactured In: United States
Units Affected: 2,800 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 · FDA Press Release · 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.