A&P Creations recalls X10 Natural Enhancement Supplement and biQ-FEL over undeclared Sildenafil and Tadalafil
The notice says X10 Natural Enhancement Supplement and biQ-FEL contain Sildenafil and Tadalafil that are not declared, and it covers 1,283 retail units and 3,116 bottles sold nationwide.
What to do
The notice does not give instructions. Read the official notice for details.
Recall details
- Product
- X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, Clermont, FL 34714.; 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
- Company
- A&p Creations
- Hazard
- Product contains undeclared Sildenafil and Tadalafil.
- Units
- 1,283 retail units; 3,116 bottles
- Where sold
- Distributed nationwide (US).
- FDA classification
- Class I · Ongoing
- Classified by FDA
- October 7, 2026
- Recall started
- September 14, 2026
- FDA enforcement report
- October 14, 2026
- Identifiers
- Codes: Lot # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.
- FDA recall number: H-0016-2027
- Codes: Lot # biQ-f001-06-25, Expiry: 05/06/2027; Lot # biQ-003-01-26, Expiry: 01/01/28
- FDA recall number: H-0017-2027
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- Product
- X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, Clermont, FL 34714. | 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
- Reason for recall
- Product contains undeclared Sildenafil and Tadalafil.
- Classification
- Class I (Ongoing)
- Distribution
- Distributed nationwide (US).
- Quantity
- 1,283 retail units; 3,116 bottles
Related recalls
Vitality Works recalls 365 Whole Foods Market Ashwagandha Capsules over possible Salmonella contamination
One lot of the 120 count capsules could be contaminated with Salmonella, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
Primal Supplements Group recalls Primal Herbs Volume herbal supplement because it contains sildenafil not on the label
FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil, which is not listed on the product label.
Evexias Health Solutions recalls Amino Ultra capsules because label fails to list fish oil
The Amino Ultra 90-capsule dietary supplement is mislabeled because its label does not declare that it contains fish oil.
Evexias Health Solution · 30 bottles
Tonight We Ride recalls Ultimate Forza Male Supplement capsules over undeclared sildenafil, tadalafil and dapoxetine
The capsules contain sildenafil, tadalafil and dapoxetine that are not listed on the label, which may interact with nitrates and lower blood pressure to dangerous levels.
Pacific Health Sciences recalls Babies' Magic Tea Baby Sleep Gripe Water over undeclared alcohols
FDA testing of one lot found ethanol, methanol and isopropanol that are not listed on the label, which may pose a risk depending on the amount consumed and the age and body weight of the person using it.
Pacific Health Sciences Llc · 953 units
Leader Formulas recalls RAPTURE Preworkout powder over undeclared DMAA found in FDA testing
FDA testing found 1,3-Dimethylamylamine (DMAA) in one lot of RAPTURE Preworkout, and using DMAA can raise blood pressure and could lead to heart problems including heart attack, shortness of breath and chest tightening.