Undeclared Viagra, Cialis Ingredients Prompt biQ-FEL Recall 2026

A dietary supplement sold nationwide through Amazon, Walmart.com and naturefuel.us can dangerously interact with common heart and blood pressure medications, according to a nationwide recall issued by A&P Creations LLC. The Clermont, Florida-based company is pulling certain lots of its biQ-FEL 500 mL liquid supplement after laboratory testing by the U.S. Food and Drug Administration found it contains undeclared sildenafil and tadalafil, the active ingredients in the prescription erectile dysfunction drugs Viagra and Cialis.

Both drugs are approved by the FDA only for use under a licensed health care provider’s supervision. When taken unknowingly, especially by people using nitrate-based medications such as nitroglycerin, they can cause blood pressure to fall to dangerous levels. Consumers managing diabetes, high blood pressure, high cholesterol or heart disease are considered especially vulnerable, since many in these groups are prescribed nitrates as part of their treatment.

What Products Are Being Recalled?

The recall covers biQ-FEL, a liquid supplement packaged in a 500 mL bottle. The label carries Spanish-language text, including the phrase ‘Sabor artificial Hierbabuena.’ Two lots are affected:

• Lot biQ-f001-06-25, expiring 05/06/27, identified on the label simply as ‘biQ-FEL’
• Lot biQ-003-01-26, expiring 01/01/28, UPC/barcode 7709799120663

The product was sold to consumers across the United States through Amazon, Walmart.com and the company’s own site, naturefuel.us.

Why Was This Recall Issued?

A&P Creations LLC distributed biQ-FEL as a finished product; the company says it did not manufacture or formulate it. The recall was triggered after FDA laboratory analysis detected sildenafil and tadalafil in the supplement, neither of which appeared on the product’s ingredient labeling. Undeclared drug ingredients in supplements marketed for sexual enhancement are a recurring concern for regulators, since consumers have no way of knowing they are being exposed to prescription-strength medication.

As of September 14, 2026, the company says it has not received any reports of adverse events tied to the product.

Who Should Be Concerned

Anyone who purchased biQ-FEL 500 mL through the listed retailers should check their bottle against the lot numbers and expiration dates above. Because the product was sold online and shipped nationwide, the FDA and the company are treating this as a nationwide recall rather than one limited to specific states.

What Consumers Need to Do Now

Consumers who have the recalled biQ-FEL 500 mL should stop using it right away and destroy the bottle rather than attempt to return it for a refund through the retailer. A&P Creations LLC says it is notifying affected customers directly through electronic notifications and through the applicable marketplace customer notification procedures.

Anyone with questions can reach the company at ecommerce@naturefuel.us, Monday through Friday from 9:00 a.m. to 4:00 p.m. ET. Consumers who experienced any symptoms after taking the product are urged to contact their physician or health care provider, and adverse events can be reported to the FDA’s MedWatch program online.

From the Agency

The FDA notes that when a company announces a recall, market withdrawal or safety alert, the agency posts the announcement as a public service and does not endorse the product or the company involved. The agency confirms this recall is being carried out with its knowledge.