FDA Recall: X10 X10 Natural Enhancement Supplement
Source: FDA
File Your Claim Now

FDA Recall: X10 X10 Natural Enhancement Supplement

X10 September 15, 2026

FDA Recall: X10 Natural Enhancement Supplement — Undeclared Sildenafil & Tadalafil

Alert for consumers: A&P Creations LLC has voluntarily recalled all lots of its X10 Natural Enhancement Supplement after U.S. Food & Drug Administration (FDA) testing found undisclosed prescription drugs—sildenafil and tadalafil. Anyone who has the product should stop using it immediately, confirm the lot number, and safely discard any remaining sachets.

Why the X10 Natural Enhancement Supplement Recall Was Issued

Sildenafil and tadalafil are the active ingredients in Viagra and Cialis. These vasodilators can sharply lower blood pressure and interact with nitrates commonly taken for heart disease. Because the drugs were not listed on the X10 Supplement label, users could unwittingly place themselves at risk for life-threatening hypotension, fainting, or cardiac events—especially if they have diabetes, hypertension, or high cholesterol.

Recalled Lots and Packaging Details

  • Presentation: Red-and-gold carton containing seven 15 mL red, lightning-bolt-shaped sachets (total 105 mL)
  • UPC: 7708075247094 (Spanish-language carton marked “X10 Bebida Energizante”)
Lot Number Expiration Date
F090824LN16 08/2026
F170325LN19 03/2027
F300326LN28 03/2028

Where X10 Natural Enhancement Supplement Was Sold

The recalled lots were distributed nationwide through the following online retailers between December 15 2024 and June 11 2026:

  • Amazon
  • Walmart.com
  • naturefuel.us

Immediate Actions for Consumers

  • Discontinue use of X10 Natural Enhancement Supplement right away.
  • Dispose of the product so it cannot be accidentally consumed by children, pets, or others.
  • Seek medical attention if you experience dizziness, fainting, chest pain, or any unexpected symptoms after taking X10.
  • Email A&P Creations LLC at ecommerce@naturefuel.us (Mon–Fri, 9 a.m.–4 p.m. ET) for refund or replacement instructions.
  • Report adverse reactions to the FDA MedWatch program at fda.gov/medwatch/report.htm or by calling 1-800-332-1088.

Source

Official Recall Images

Retail box of X10 Natural Enhancement Supplement
Source: FDA
Red lightning-bolt sachets of X10 Natural Enhancement Supplement
Source: FDA

Frequently Asked Questions

Why is the X10 Natural Enhancement Supplement being recalled?
FDA laboratory analysis detected undeclared sildenafil and tadalafil, ingredients that can dangerously lower blood pressure when taken without medical supervision.
How can I confirm if my X10 Natural Enhancement Supplement is part of the recall?
Match the lot number on your package with the recalled lots: F090824LN16 (exp 08/2026), F170325LN19 (exp 03/2027), or F300326LN28 (exp 03/2028).
What should I do with my recalled X10 Natural Enhancement Supplement sachets?
Stop using them immediately and discard the sachets in a way that prevents accidental ingestion. Then contact A&P Creations LLC for a refund or replacement.
Have any illnesses linked to X10 Natural Enhancement Supplement been reported?
No adverse events had been reported to A&P Creations LLC as of September 14 2026, according to the FDA notice.
How do I report side effects from X10 Natural Enhancement Supplement to the FDA?
Submit a report through MedWatch (fda.gov/medwatch/report.htm) or call 1-800-332-1088 for a paper form.
Is it safe to continue using X10 Natural Enhancement Supplement if I have no heart problems?
No. The presence of undisclosed prescription drugs means the product is unsafe for all users, regardless of existing medical conditions.
Are there safer alternatives to X10 Natural Enhancement Supplement?
Consult your healthcare provider about FDA-approved treatments for erectile dysfunction. Only take medicines that list ingredients clearly and have been prescribed by a licensed professional.

File Your Claim Now