All Lots of Rhino 7 3000 and Rhino 7 Platinum 3000 Capsules Recalled Nationwide

Posted on October 11, 2015 by


TF Supplements of Houston, TX, is recalling the following product to the consumer level: RHINO 7 3000 capsules packaged in a bottle containing six (6) capsules UPC: 616453150126 ALL LOT NUMBERS WITHIN EXPIRY and Rhino 7 Platinum 3000 Capsules packaged in a single (1) blister packs hang card count UPC: 700729253748 ALL LOT NUMBERS WITHIN EXPIRY. Lot numbers are on the back top right of the (1) count and on the side of the (6) count bottle. FDA analysis found these products to contain undeclared desmethyl carbondenafil and dapoxetine. Desmethyl carbondenafil is a phosphodiesterase PDE-5 inhibitor which is a class of drugs used to treat male erectile dysfunction, making these products unapproved new drugs. Dapoxetine is an active ingredient not approved by the U.S. Food and Drug Administration (FDA).

TF Supplements has received a report of one (1) adverse event associated with these products to date.

These products are marketed as dietary supplements for sexual enhancement and packaged in (6) count bottle and (1) count hanging card and distributed to consumers nationwide via our retail website TF Supplements has discontinued sales of these products.

TF Supplements is notifying its customers via e-mail of this voluntary recall. Consumers that purchased these products from TF Supplements should stop using them immediately and can return the products to:

TF Supplements
6666 Gulf Freeway
Houston, TX 77087

Consumers with questions regarding this recall can contact TF Supplements by telephone at 866-620-3586 between (Monday – Friday 9:00am to 5:00pm CST). Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these products.

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Posted in: Family safety