On September 14, 2026, Clermont, Florida-based A&P Creations LLC announced two nationwide consumer-level recalls after FDA laboratory analysis found undeclared sildenafil and tadalafil — the active ingredients in Viagra and Cialis — in products sold as natural supplements. The FDA published both announcements on September 15. The recalled items are X10 Natural Enhancement Supplement and biQ-FEL, and both were distributed through Amazon, Walmart.com and the company's naturefuel.us storefront.

Why It Matters

Spiked supplements are the shadow market that legitimate male sexual health companies compete against, and this pair of recalls is a clean illustration of why the economics favour the bad actors. A telehealth ED platform pays for a prescriber, a pharmacy relationship and a compliance function; a marketplace seller drop-shipping an unregulated liquid pays for a box design. Both reach the same consumer through the same Amazon search — except one of them has been quietly dosing him with two PDE5 inhibitors at unknown concentrations for eighteen months. The marketplace angle is the part the industry should sit with. This did not move through gas-station racks or a sketchy affiliate funnel; it moved through Amazon and Walmart.com, the two retail surfaces that mainstream sexual wellness brands have spent a decade fighting to get shelf space on. Brand-gating and restricted-category rules have made it hard for compliant vibrator and lubricant brands to list, while a Spanish-labelled "energy beverage" with a lightning bolt on the box sold for a year and a half. For the legitimate end of the market — Promescent, Hims, Ro, the supplement brands making conservative claims — every one of these recalls raises the FTC and FDA temperature on the whole category's advertising, and reinforces the consumer suspicion that "natural" is a synonym for "unlabelled pharmaceutical."

The X10 recall is the larger of the two. The product is a liquid sold in a red-and-gold box holding seven red lightning-bolt-shaped 15 mL sachets (105 mL total), UPC 7708075247094, with Spanish-language packaging describing it as a "Bebida energizante" — an energy beverage. Three lots are affected: F090824LN16 (exp. 08/2026), F170325LN19 (exp. 03/2027) and F300326LN28 (exp. 03/2028). The affected product was distributed to U.S. consumers between December 15, 2024 and June 11, 2026 — an eighteen-month sales window. The companion biQ-FEL recall covers a 500 mL liquid supplement bottle, also Spanish-labelled ("Sabor artificial Hierbabuena"), across lots biQ-f001-06-25 (exp. 05/06/27) and biQ-003-01-26 (exp. 01/01/28), UPC 7709799120663.

The safety rationale is the standard one for spiked sexual-enhancement products, and it is not theoretical. As the FDA notice states, these undeclared ingredients "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." That is precisely the comorbidity profile of the men most likely to buy an over-the-counter erection product rather than see a doctor. As of September 14, A&P Creations had received no reports of adverse events tied to either recall.

One detail worth flagging: A&P Creations states it "purchased and distributed X10 Natural Enhancement Supplement as a finished product and did not manufacture or formulate the product." The same disclaimer appears in the biQ-FEL notice. The company initiated both recalls after the FDA's own lab analysis, not its own testing. Consumers are told to stop use immediately and destroy the product; the company is reachable at [email protected].

Sources

Update — 2026-09-17

Initial entry — story first created.