biQ-FEL and X10 Supplements Recalled Nationwide After FDA Finds Hidden Viagra and Cialis Ingredients

What A&P Creations Is Recalling, and Why It Matters

If anyone in your household has bought a sexual enhancement product online, it is worth a few minutes to check whether it is one of the two products named in this recall. A&P Creations LLC, a company based in Clermont, Florida, announced on September 14 that it is recalling both products to the consumer level because laboratory analysis by the U.S. Food and Drug Administration found drug ingredients that were not listed on their labels.

The two products are biQ-FEL, sold in a 500 mL liquid bottle, and X10 Natural Enhancement Supplement, a liquid sold in sachets. According to the company's announcements, both were found to contain undeclared sildenafil and tadalafil, the active ingredients in the FDA-approved prescription drugs Viagra and Cialis, which are used to treat erectile dysfunction. The FDA listed both recalls on its website on September 15.

A&P Creations says it distributed both products as finished goods and did not manufacture or formulate either one, and that it decided to recall them after the FDA's laboratory analysis. Both recalls are being conducted with the knowledge of the U.S. Food and Drug Administration.

The Danger for People Who Take Nitrates

Both A&P Creations announcements and the FDA's own warnings about the two products carry the same caution: these undeclared ingredients may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. The notices add that people with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates. They also point out that FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional.

How to Tell If You Have the Recalled biQ-FEL

The recalled biQ-FEL is a liquid packaged in a 500 mL bottle bearing the biQ-FEL name. According to A&P Creations, the product label includes Spanish-language text, including “Sabor artificial Hierbabuena,” and the product was distributed to consumers in the United States through Amazon, Walmart.com and naturefuel.us. The specific lots named in the notice are:

• Lot biQ-f001-06-25, expiration date 05/06/27, with the UPC or barcode identifier given in the notice as biQ-FEL
• Lot biQ-003-01-26, expiration date 01/01/28, UPC 7709799120663

The FDA published a warning advising consumers not to purchase or use biQ-FEL, which it said was promoted for sexual enhancement on various websites, including walmart.com and biqfelusa.com, and possibly in some retail stores. In that warning, the agency said its laboratory analysis confirmed that biQ-FEL contains sildenafil and tadalafil not listed on the product label.

How to Tell If You Have the Recalled X10

X10 Natural Enhancement Supplement is described in the company's notice as a liquid product packaged in a red and gold box containing 7 red lightning bolt-shaped sachets, 15 mL each, for a total of 105 mL, with UPC 7708075247094. The original Spanish-language package identifies the product as “X10” and describes it as “Bebida energizante,” which the notice translates as energy beverage. The affected lots are:

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

A&P Creations says the affected product was distributed to consumers in the United States through Amazon, Walmart.com and naturefuel.us between December 15, 2024, and June 11, 2026. On May 29, 2026, the FDA published a warning advising consumers not to purchase or use X10 Natural Enhancement Supplement, which it said was promoted for sexual enhancement on various websites, including naturefuel.us, and possibly in some retail stores. The agency said its laboratory analysis confirmed that the product contains sildenafil and tadalafil not listed on the product label.

What the Company Tells Consumers to Do

Neither notice offers a refund or a way to send the product back, and the instruction in both is to get rid of it. For biQ-FEL, A&P Creations says consumers who have the recalled 500 mL product should stop using it immediately and are urged to destroy it, and for X10, the company says consumers are urged to stop using the product immediately and destroy or dispose of it.

The company has stopped distributing both products and says it is notifying affected customers through direct electronic notifications and through the customer notification procedures of the marketplaces where the products were sold. For questions about either recall, A&P Creations gives one contact, the email address [email protected], answered Monday through Friday from 9:00 a.m. to 4:00 p.m. Eastern Time, and neither notice lists a company telephone number.

If You Have Already Been Taking It

A&P Creations states that as of September 14, it had not received any reports of adverse events related to either recall. Both notices give the same advice: consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using the product.

Both notices say that bad reactions or quality problems can be reported to the FDA's MedWatch Adverse Event Reporting Program using the MedWatch online reporting form. The X10 notice adds that a reporting form can be downloaded from the FDA's MedWatch reporting page or requested by calling 1-800-332-1088, then returned to the address on the pre-addressed form or faxed to 1-800-FDA-0178.

What the FDA Says About Products Like These

In its warnings about both products, the FDA said its notifications are meant to inform the public of products potentially marketed as dietary supplements or conventional foods with hidden drug ingredients and chemicals. The agency said such products are typically promoted for sexual enhancement, weight loss, pain relief and body building, are often represented as being all natural, and call for caution before anyone buys them. It also said it is unable to test and identify all products marketed as dietary supplements that have potentially harmful hidden ingredients.