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Class II FDA

X10 Natural Enhancement Supplement recalled over Undeclared drug ingredient

Status: Ongoing · Recalled September 14, 2026 · Updated September 25, 2026
X10 Natural Enhancement Supplement was recalled on September 14, 2026 because of undeclared drug ingredient. It is a Class II recall (possible temporary or reversible harm). Affected area: nationwide. Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
HazardUndeclared drug ingredient
Risk levelClass II
Affected areaNationwide
CategoryFood

What to do

Do not eat this product. Check the official FDA notice for affected lot codes and instructions.

Confirm the details against the official FDA notice before acting.

Does this affect you?

Check the product in your home against the recalled item:

Product as filed
A&P Creations LLC — Nationwide Recall of X10 Natural Enhancement Supplement Due to Undeclared Sildenafil and Tadalafil
UPC / code
7708075247094
Sold at
Walmart.com

Full recall details

Reason for recall
Clermont, Florida – A&P Creations LLC is recalling X10 Natural Enhancement Supplement to the consumer level because it has been found to contain undeclared sildenafil and tadalafil.
Hazard class
Class II — possible temporary or reversible harm
Recalling company
A&P Creations LLC
Recall type
Voluntary
Quantity
Distribution
The affected product was distributed to consumers in the United States through Amazon, Walmart.com, and naturefuel.us between December 15, 2024 and June 11, 2026. A&P Creations LLC purchased and distributed X10 Natural Enhancement Supplement as a finished product and did not manufacture or formulate the product.

Frequently asked questions

Is X10 Natural Enhancement Supplement recalled?

Yes. It was recalled on September 14, 2026 because clermont, Florida – A&P Creations LLC is recalling X10 Natural Enhancement Supplement to the consumer level because it has been found to contain undeclared sildenafil and tadalafil.

What should I do if I have it?

Do not eat this product. Check the official FDA notice for affected lot codes and instructions.

Which states are affected?

This recall is nationwide.

How do I identify the recalled product?

Look for: UPC 7708075247094.

How serious is a Class II recall?

Class II means possible temporary or reversible harm.

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