X10 Supplement Sold On Amazon And Walmart Recalled Nationwide Over Hidden Viagra And Cialis Ingredients

(MENAFN- Grocery Coupon Guide) A liquid supplement sold through Amazon and Walmart is being recalled nationwide after federal testing found prescription drug ingredients that weren't disclosed on the product's label.

A&P Creations LLC of Clermont, Florida, is recalling three lots of X10 Natural Enhancement Supplement after U.S. Food and Drug Administration laboratory testing detected sildenafil and tadalafil. Those are the active ingredients in the FDA-approved prescription erectile dysfunction drugs Viagra and Cialis, respectively.

The FDA says consumers should stop using the recalled X10 product immediately because the hidden ingredients can interact with certain medications and potentially cause dangerously low blood pressure.

The company reported no adverse events associated with the recall as of September 14, 2026.

Which X10 Products Are Recalled?

The recall involves X10 Natural Enhancement Supplement packaged as a liquid in a red-and-gold box.

Each box contains seven red lightning bolt-shaped 15-milliliter sachets, for a total of 105 milliliters. The Spanish-language packaging identifies the product as“X10” and describes it as“Bebida energizante,” or energy beverage.

The UPC is 7708075247094.

Consumers should check for these three recalled lot and expiration-date combinations:

Lot F090824LN16 - Expiration 08/2026 Lot F170325LN19 - Expiration 03/2027 Lot F300326LN28 - Expiration 03/2028

The affected product was distributed to consumers in the United States through Amazon, Walmart, and naturefuel between December 15, 2024, and June 11, 2026.

That means shoppers who bought X10 online during that period may want to check their marketplace order history as well as any remaining product they have at home.

Why FDA Says the Hidden Ingredients Are Dangerous

The concern isn't simply that the product's label was incomplete.

FDA laboratory analysis found sildenafil and tadalafil, prescription drug ingredients that require medical supervision and weren't listed on X10's labeling.

The drugs can interact with nitrates found in certain prescription medications, including nitroglycerin, and potentially cause blood pressure to fall to dangerous levels.

FDA specifically notes that people with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates, making the undisclosed ingredients particularly concerning for people who don't realize they're consuming them.

The agency had already issued a consumer warning about X10 Natural Enhancement Supplement on May 29 after its laboratory testing confirmed the hidden ingredients.

FDA Warns About a Broader Problem With Enhancement Products

X10 isn't the only product that has prompted this type of federal warning.

FDA maintains a list of sexual enhancement and energy products found with hidden ingredients, and the agency warns that many products marketed for sexual enhancement or sexual dysfunction may contain potentially dangerous undisclosed substances.

Some are promoted as dietary supplements, foods, or“all-natural” alternatives and can be sold both online and in physical stores.

FDA also cautions that its database represents only a fraction of potentially hazardous products on the market. A product's absence from the agency's warning list therefore shouldn't be interpreted as proof that it is safe.

Consumers considering sexual-enhancement supplements should be particularly cautious about products promising prescription-like effects without requiring medical supervision.

Distributor Says It Did Not Manufacture X10

A&P Creations says it purchased and distributed X10 as a finished product and did not manufacture or formulate it.

The company initiated the recall after FDA laboratory analysis identified sildenafil and tadalafil that weren't declared on the product labeling.

A&P Creations has since stopped distributing X10 and says it is notifying affected customers through direct electronic communications and marketplace customer-notification procedures.

The recall is being conducted with FDA's knowledge.

What Shoppers Should Do With Recalled X10

Consumers who have one of the recalled X10 lots should stop using the product immediately and destroy or dispose of it, according to the company's recall announcement.

Anyone who purchased X10 through Amazon or Walmart can also check their online order history to determine when the product was purchased and compare any product still on hand with the recalled lot numbers.

Consumers with questions about the recall can contact A&P Creations LLC at [email protected] Monday through Friday from 9 a.m. to 4 p.m. Eastern Time.

Anyone who believes they experienced a health problem after using X10 should contact a physician or other healthcare provider.

Consumers and healthcare professionals can also report adverse reactions or product-quality problems through the FDA MedWatch program.

The most important step for shoppers is to check the lot number, not simply the product name. Three specific X10 lots are included in the nationwide recall, and two of them carry expiration dates extending into 2027 and 2028.

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