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FDA recall,

Rhino Choco VIP 10X Chocolate

Rhino Choco VIP 10X Chocolate contains undeclared Tadalafil, which may lower blood pressure to dangerous levels.

What happened

USA LESS Co. is recalling Rhino Choco VIP 10X Chocolate because it contains undeclared Tadalafil, which is not listed on the product label. Tadalafil is the active ingredient in Cialis, an FDA-approved prescription drug used to treat erectile dysfunction.

The undeclared ingredient may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates. The product is sold in retail stores and through on-line sites.

The company announced the recall on February 27, 2026, and has immediately removed the product from its online store until the problem is corrected.

What to do

If a code on your package is listed below:

  1. Consumers who have purchased Rhino Choco VIP 10x from usaless.com are urged to immediately return them to the place of purchase for a full refund.
  2. Consumers with questions may contact the company at 1-800-872-5377 or 409749@email4pr.com. 1-800-872-5377. 409749@email4pr.com.

Is yours affected?

Match the UPC and expiration date listed under your product.

A UPC is the number printed under a barcode.

  1. Rhino Choco VIP 10X

    UPC
    • 724087947668
    Expiration date
    10/2027

From the FDA notice

BROOKLYN, N.Y., Feb. 27, 2026 /PRNewswire/ -- USALESS.COM is recalling its RHINO CHOCO VIP 10X, in 10 gr, 12 pc packages that come in a black cardboard box marked with UPC Code 724087947668 on the back and with an expiration date of 10/2027 stamped on the back.

10X, in 10 gr, 12 pc packages that come in a black cardboard box marked with UPC Code 724087947668 on the back and with an expiration date of 10/2027 stamped on the back.

Recall details

Company announced
Sold in

The product is sold in retail stores and through on-line sites.

Company
USA LESS Co.

Summary by Recall Canary, written with AI · summary updated Oct 2, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)