Hidden Viagra, Cialis Ingredients Trigger Recall of X10 Supplement 2026

A hidden dose of prescription-strength erectile dysfunction medication is at the center of a new nationwide recall. A&P Creations LLC, based in Clermont, Florida, is pulling its X10 Natural Enhancement Supplement from consumers after FDA laboratory testing found the product secretly contains sildenafil and tadalafil, the active ingredients in Viagra and Cialis.

Neither ingredient was listed on the product label. Because Viagra and Cialis are FDA-approved prescription drugs meant to be taken only under a doctor’s supervision, finding them undeclared in an over-the-counter supplement raises serious safety concerns, especially for people taking other medications that were never meant to interact with them.

Why Was This Recall Issued?

According to the company’s announcement, A&P Creations LLC decided to recall the product after FDA lab analysis confirmed the presence of sildenafil and tadalafil, neither of which appeared on the packaging. The company says it purchased and distributed X10 as a finished product and did not manufacture or formulate it itself.

Sildenafil and tadalafil can interact dangerously with nitrates found in some prescription drugs, such as nitroglycerin, potentially lowering blood pressure to unsafe levels. People managing diabetes, high blood pressure, high cholesterol, or heart disease are frequently prescribed nitrates, putting them at heightened risk if they unknowingly combine those medications with X10.

What Products Are Being Recalled?

The recalled item is X10 Natural Enhancement Supplement, a liquid product sold in a red and gold box containing seven red lightning bolt-shaped sachets, each holding 15 mL, for a total of 105 mL per box. The UPC listed is 7708075247094. Notably, the original Spanish-language packaging labels the product simply as ‘X10’ and describes it as a ‘Bebida energizante,’ or energy beverage.

Three lots are affected by the recall:

• Lot F090824LN16, expiring 08/2026
• Lot F170325LN19, expiring 03/2027
• Lot F300326LN28, expiring 03/2028

Who Is Affected?

A&P Creations LLC distributed X10 to consumers across the United States through Amazon, Walmart.com, and the company’s own site, naturefuel.us. The affected sales window runs from December 15, 2024 through June 11, 2026, meaning anyone who purchased the supplement online during that stretch should check their order history and product on hand.

As of the September 14, 2026 announcement, the company reports it has not received any adverse event reports connected to this recall. Still, given the nature of the undeclared ingredients, health officials are urging caution rather than waiting for reported harm.

What Should You Do?

If you have X10 Natural Enhancement Supplement in your home, stop using it right away. The company is advising consumers to destroy or dispose of the product rather than attempt to return it for a refund through normal channels. A&P Creations LLC says it has already ceased further distribution and is reaching out to known customers directly through electronic notifications, along with notification procedures required by the marketplaces where it sold the product.

Anyone who has taken X10 and experienced symptoms that could be linked to the undeclared medications, such as an unexpected drop in blood pressure, dizziness, or interactions with heart or blood pressure medication, should contact a physician or healthcare provider promptly. Consumers with questions about the recall can reach A&P Creations LLC at ecommerce@naturefuel.us, Monday through Friday from 9:00 a.m. to 4:00 p.m. Eastern Time.

Regulatory Response

The FDA notes that this recall is being carried out with its knowledge, and the agency is encouraging anyone who experienced an adverse reaction or quality issue with the product to file a report through its MedWatch Adverse Event Reporting Program, either online or by calling 1-800-332-1088 to request a paper form.

As with any recall involving undisclosed pharmaceutical ingredients in a supplement, health authorities stress that consumers cannot visually identify the contamination. The safest step is simply to stop use and dispose of any remaining product rather than risk continued exposure.