Select Distributions LLC is recalling 60 boxes of Aphrodisiac Platinum 40000 (Proprietary Raw Material 6000 mg) because FDA analysis found the product contains sildenafil. Sildenafil is the active ingredient in a prescription drug for erectile dysfunction, and this product was marketed as a dietary supplement without required FDA approval. The product was sold in 1-count blister cards (24 cards per box) and distributed in Michigan and Ohio. Consumers are advised to contact their healthcare provider or pharmacist for guidance and return any unused product to the place of purchase for a refund.
Undeclared sildenafil can interact with nitrates found in some prescription drugs, such as nitroglycerin, which may lower blood pressure to dangerous or life-threatening levels. This is particularly hazardous for people with heart disease, diabetes, high blood pressure, or high cholesterol who often take prescription nitrates.
Return to place of purchase for a refund.
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 · Raw API Response
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