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.
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.
Healthcare consultation and refund

Label, The Beast
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.
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.