AMA Wholesale is recalling all lots of Rhino 69 Extreme 50000, sold in single-capsule blister packs, because FDA testing discovered the product contains undeclared tadalafil. Tadalafil is an active ingredient found in FDA-approved prescription drugs for erectile dysfunction, but its presence in this product was not disclosed on the label. This makes the product an unapproved drug for which safety and effectiveness have not been established. Consumers should immediately stop using this product and contact their healthcare provider or pharmacist for guidance on any health concerns.
Undeclared tadalafil can interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to life-threatening levels. This pose a significant risk to individuals with heart disease, high blood pressure, diabetes, or high cholesterol who frequently take prescription nitrates.
Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy 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
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.