SUPPLEMENT RECALL — COMMUNITY & ACCESS
Check the lot. X10 and biQ-FEL supplements sold online contain undeclared prescription-drug ingredients.
The recall covers three X10 lots and two biQ-FEL lots distributed through Amazon, Walmart.com and naturefuel.us. Stop using an exact match. Do not assume the numeric biQ-FEL barcode applies to both recalled lots: FDA publishes it for only one.
Match the product, lot and expiration
- X10 Natural Enhancement Supplement: red-and-gold box with seven 15 mL sachets; UPC
7708075247094. - X10 lot
F090824LN16: expires 08/2026. - X10 lot
F170325LN19: expires 03/2027. - X10 lot
F300326LN28: expires 03/2028. - biQ-FEL: 500 mL bottle marked “Sabor artificial Hierbabuena.”
- biQ-FEL lot
biQ-f001-06-25: expires 05/06/27. FDA's barcode cell says “biQ-FEL”; it does not publish a numeric barcode for this row. - biQ-FEL lot
biQ-003-01-26: expires 01/01/28; barcode7709799120663. - If it matches: stop using it immediately.
Why the missing ingredients matter
FDA testing found sildenafil and tadalafil in both products. Those prescription drugs are used to treat erectile dysfunction, but neither ingredient is declared on these supplement labels.
The announcements warn that sildenafil and tadalafil can interact with nitrates such as nitroglycerin and lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates and may face particular risk from that interaction.
A&P Creations reported no related adverse events as of September 14. That is not a statement that a recalled package is safe to keep using.
What to do with a match
The company tells consumers to stop using the products and destroy or dispose of them. The announcements do not give a product-specific method, return route or refund process. This guide therefore does not tell readers to put a package in household trash, pour liquid down a drain or bring it to a retailer.
For product questions, email ecommerce@naturefuel.us. The company lists assistance Monday through Friday from 9 a.m. to 4 p.m. Eastern. If you experienced a problem that may be related to either product, contact a healthcare professional. FDA also accepts reports through MedWatch ↗.
One FDA identifier row remains imperfect
For biQ-FEL lot biQ-f001-06-25, the FDA-posted table repeats the product name in the “UPC/Barcode Identifier” field instead of giving a number. That is a limitation in the controlling public record—not a reason to copy the second lot's barcode onto the first. Use the product name, bottle size, lot and expiration together, and contact the company if any marking is unclear.
Online distribution is confirmed; a Rockland purchase is not
The company announcements say the products were distributed in the United States through Amazon, Walmart.com and naturefuel.us. That creates a concrete check for Rockland residents who ordered either product online, but it does not establish a Rockland sale, purchaser, adverse event or medical outcome.
What changes for a resident: check X10 and biQ-FEL packages against the exact lot and expiration lists above, stop using a match, and do not extend the one published biQ-FEL barcode to the lot for which FDA gives no numeric barcode.
Primary sources: FDA-posted X10 company announcement ↗ and FDA-posted biQ-FEL company announcement ↗, both company-dated September 14 and FDA-published September 15, 2026. Product descriptions, lots, expirations, barcodes, ingredients, risks, consumer instruction, contact route and distribution channels were rechecked September 15, 2026, at 7:55 p.m. EDT. FDA posts company announcements as a public service and does not endorse the products or company.