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Rhino 69 Extreme 50000 recalled

The sexual enhancement product contains tadalafil, which is not declared on the label

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AMA Wholesale is recalling Rhino 69 Extreme 50000 capsules.

FDA analysis found the product to be tainted with tadalafil, an active ingredient in a FDA-approved prescription drug used for erectile dysfunction, which is not declared on the label.

The firm has not received any reports of adverse events related to this recall.

The recalled product, which is used as a sexual enhancer and packaged in single capsule, blister packs with an expiration date of 12/2022 and UPC Code: 718122071128, was sold nationwide on the internet.

What to do

Customers who purchased the recalled product should immediately stop using it and return it to the place of purchase for a refund.

Consumers with questions may contact the company at (800) 689-6532 Monday through Friday from 9:00 am to 5:00 pm (PST) or by email at

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