The X10 Natural Enhancement recall is now a nationwide consumer-level recall after FDA laboratory testing identified undeclared sildenafil and tadalafil in the product. A&P Creations is recalling three X10 lots, and consumers with recalled product are being told to stop using it immediately and destroy or dispose of it.
This is a later and more actionable state than FDA’s earlier May 29 warning about hidden drug ingredients. The September recall adds a defined lot scope, distribution history and direct consumer action.
Direct answer: Check the X10 package and lot number. If it matches one of the recalled lots below, stop using it immediately and destroy or dispose of it. If you experienced a health problem after using X10, contact a physician or other healthcare provider and consider reporting the problem through FDA MedWatch.
Which X10 Natural Enhancement lots are recalled?
| Lot | Expiration |
|---|---|
| F090824LN16 | 08/2026 |
| F170325LN19 | 03/2027 |
| F300326LN28 | 03/2028 |
FDA describes the recalled product as X10 Natural Enhancement Supplement in a red-and-gold box containing seven red lightning-bolt-shaped 15 mL sachets, 105 mL total. The UPC listed in the recall is 7708075247094.
Where was the recalled X10 sold?
The affected product was distributed in the United States through Amazon, Walmart.com and naturefuel.us between December 15, 2024 and June 11, 2026.
That distribution window does not by itself prove that every X10 package purchased during that period is one of the three recalled lots. The safest verification step is to match the package and lot details against the FDA recall notice.
Why is X10 being recalled?
FDA laboratory analysis found undeclared sildenafil and tadalafil. These are prescription drug ingredients used in erectile-dysfunction medicines and were not declared on the X10 product labeling.
FDA warns that products containing undeclared sildenafil or tadalafil can interact with nitrates such as nitroglycerin and may lower blood pressure to dangerous levels. The risk is particularly important because a consumer may not know the prescription ingredients are present.
What should you do if you have recalled X10?
Compare the lot number and package details with the recalled lots listed above.
FDA’s recall notice says consumers with recalled product should stop use immediately.
The company recall instructs consumers to destroy or otherwise dispose of the affected product.
If you experienced a problem that may be related to using X10, contact a physician or healthcare provider.
FDA provides the MedWatch program for reporting adverse reactions or quality problems associated with the product.
Were any adverse events reported?
A&P Creations said it had received no reports of adverse events related to the recalled product as of September 14, 2026.
That statement is time-bounded. It does not mean adverse events cannot occur, that later reports will not be filed or that the product is safe for consumers who are not taking nitrates.
Was X10 already under an FDA warning?
Yes. FDA had already warned consumers on May 29, 2026 not to purchase or use X10 Natural Enhancement after laboratory analysis detected hidden sildenafil and tadalafil.
The September recall is the material new state. It moves the product from a public health-fraud warning into a formal consumer-level recall with identified lots and direct stop-use and disposal instructions.
Has X10 been removed from Amazon and Walmart?
The recall notice says distribution has ceased and that A&P Creations is notifying affected customers through direct electronic and marketplace procedures. TPS did not establish that removal is complete across every marketplace listing, seller account or previously purchased unit.
What remains unresolved?
The exact number of purchasers or units affected was not established in the reviewed evidence. Complete marketplace-removal timing is also unknown. FDA may later classify, expand, update or terminate the recall, and any later adverse-event information would materially change the current record.
Verification method
ThePulseSignal reviewed the FDA September recall notice and the earlier FDA X10 hidden-drug warning, then checked current secondary recall coverage to distinguish the May warning state from the September consumer-level recall and preserve the exact product, lot, distribution and stop-use boundaries.
