FDA recall, , High risk
A&P Creations biQ-FEL and X10 Natural Enhancement Supplements
BiQ-FEL contains undeclared Sildenafil and Tadalafil, which may lower blood pressure to dangerous levels.
Summary by Recall Canary from the FDA notice
What happened
A&P CREATIONS, of Clermont, Florida, recalled biQ-FEL and X10 Natural Enhancement Supplement because the products contain undeclared Sildenafil and Tadalafil. The recall began September 14, 2026, and the FDA added it to the Enforcement Report on October 2, 2026. The products were distributed nationwide in the US.
What to do
If a code on your package is listed below:
- Consumers who have the recalled biQ-FEL 500 mL product should stop using it immediately and are urged to destroy the product.
- Consumers with questions regarding this recall may contact A&P Creations LLC at ecommerce@
naturefuel.us Monday to Friday from 9:00 am to 4:00 pm ET. - Contact your physician or healthcare provider if you have experienced any problems that may be related to taking or using this product.
Is yours affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
A UPC is the number printed under a barcode.
X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box
- UPC
- 7708075247094
- Lot code
- F090824LN16
- F170325LN19
- 300326LN28
X10 is a liquid product
Product details from the notice
X10 is a liquid product packaged in a red and gold box containing 7 red lightning bolt-shaped sachets, 15 mL each (105 mL total), with UPC 7708075247094. The original Spanish-language package identifies the product as “X10” and describes it as “Bebida energizante” (energy beverage).
X10 is a liquid product packaged in a red and gold box containing 7 red lightning bolt-shaped sachets, 15 mL each (105 mL total), with UPC 7708075247094. The original Spanish-language package identifies the product as “X10” and describes it as “Bebida energizante” (energy beverage).: lot and date combinations Lot code Best-by or expiration date F090824LN16 08/2026 F170325LN19 03/2027 F300326LN28 03/2028 biQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle, Manufactured by Almenat SAS AV 39 Oeste No 10 Oeste-18 Cali Valle Industria Colombiana; Distributed by: Biofel
- Lot code
- biQ-f001-06-25
- biQ-003-01-26
Recall details
- Company began the recall
- Sold in
Distributed nationwide (US).
- Company
- A&P CREATIONSClermont, Florida
- Hazard
- Hidden drug ingredient
- Risk
High risk
There is a reasonable chance that taking it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 99872
- Recall numbers
- H-0016-2027 to H-0017-2027
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall · Announced by the company
Listed on Recall Canary
Added to FDA's Enforcement Report
Classified by FDA
Summary updated
In FDA's weekly enforcement report
