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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

Stiff Boy LLC: The Beast Capsules Recalled for Undeclared Sildenafil

Agency Publication Date: May 30, 2019
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Summary

Stiff Boy LLC is recalling 1,000 boxes of 'The Beast' dietary supplement capsules because they contain sildenafil, an undeclared ingredient. The Beast is sold in packets containing 4,600 mg capsules (4 per packet) and was distributed nationwide. This recall was initiated after FDA laboratory analysis discovered the presence of the drug ingredient, which is not listed on the product label. Consumers should stop using this product immediately and contact their healthcare provider or pharmacist, especially if they have experienced any adverse effects.

Risk

The undeclared sildenafil can interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. This poses a significant health risk to consumers with high blood pressure, heart disease, or diabetes, who often take nitrates.

What You Should Do

  1. Identify the product by checking for 'The Beast' capsules in 4600 mg x 4-capsule packets.
  2. Check your supply for any lot of 'The Beast' as all lots are included in this recall.
  3. Immediately stop using the product even if you have not experienced symptoms.
  4. Contact your healthcare provider or pharmacist for guidance regarding the use of this product and any potential health concerns.
  5. Return any unused capsules to the place of purchase for a full refund.
  6. Contact Stiff Boy LLC for further instructions regarding the disposal or return of the product.
  7. For additional questions, 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

Healthcare consultation and refund

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

Affected Products

Product: The Beast (4600 mg X 4 Capsules per packet)
Model:
Recall #: D-1321-2019
Lot Numbers:
All lots

Product Images

Label, The Beast

Label, The Beast

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 82704
Status: Resolved
Manufacturer: Stiff Boy LLC
Manufactured In: United States
Units Affected: 1000 boxes
Distributed To: Nationwide
Agency Last Updated: January 21, 2020

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.