Stop using now Food recall · FDA · Published September 14, 2026

A&P Creations Recalls X10 Supplement Due to Undeclared Drugs

A&P Creations recalls X10 Natural Enhancement Supplement because it contains undeclared Sildenafil and Tadalafil. Check your lot numbers.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-0016-2027Food A&P Creations ›

Stop using this now

Product contains undeclared Sildenafil and Tadalafil.

✎ GovInfoNow plain-language explainer

A&P Creactions is recalling the X10 Natural Enhancement Supplement because the product contains undeclared active pharmaceutical ingredients, specifically Sildenafil and Tadalafil. These are prescription drugs typically used to treat erectile dysfunction and pulmonary hypertension, but their presence in a supplement without disclosure poses health risks to consumers who may have contraindications or be taking other medications. The recall affects 1,283 retail units distributed nationwide. Read more at govinfonow.com/recall/1614171-a-p-creations-recalls-x10-natural-enhancement-supplement-0-5.

Source Summary by GovInfoNow · govinfonow.com/recall/1614171-a-p-creations-recalls-x10-natural-enhancement-supplement-0-5 · Published October 21, 2026 · Updated October 21, 2026 · Official notice: FDA #H-0016-2027

Cite this page

“A&P Creations Recalls X10 Supplement Due to Undeclared Drugs.” GovInfoNow, updated October 21, 2026. https://govinfonow.com/recall/1614171-a-p-creations-recalls-x10-natural-enhancement-supplement-0-5. Based on FDA recall #H-0016-2027.

A&P CREATIONS voluntarily recalled X10 Natural Enhancement Supplement nationwide on Sept. 14, 2026, after the FDA found undeclared Sildenafil and Tadalafil, according to the FDA.

How to tell if you have it

Brand: A&P Creations
Product: X10 Natural Enhancement Supplement
Size: 0.5 fl oz/sachet (15 mL), 7 sachets/box
UPC: 7708075247094
Lot # F090824LN16, Expiry: 8/2026
Lot # F170325LN19, Expiry: 03/2027
Lot # 300326LN28, Expiry: 03/2028

The hazard

The product contains undeclared Sildenafil and Tadalafil. The FDA classified the recall as Class I.

Context

GovInfoNow's records show other recent recalls of similar products include Red Bull Extreme Male Enhancement Supplement Recall (2026-03-13), Pure Vitamins recalls Boner Bears Honey male enhancement product with undeclared sildenafil and tadalafil (2026-03-13), and Blue Bull Male Enhancement Supplement Recall (2026-03-13).

How to tell if you have this one

Look for the product name 'X10 Natural Enhancement Supplement' sold in boxes of 7 sachets (0.5 fl oz each). Check the UPC code: 7708075247094. Verify the lot number and expiry date against these three specific lots: Lot # F090824LN16 (Expiry: 8/2026), Lot # F170325LN19 (Expiry: 03/2027), or Lot # 300326LN28 (Expiry: 03/2028).

Brand
A&P Creations
Category
Food

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class I
Status
Ongoing
Distribution
Distributed nationwide (US).

Recall number	Product, codes & lots	Quantity
H-0016-2027	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.; Lot # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.	1,283 retail units
H-0017-2027	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 # biQ-f001-06-25, Expiry: 05/06/2027; Lot # biQ-003-01-26, Expiry: 01/01/28	3,116 bottles

Based on the official FDA remedy

What to do — step by step

Stop Using the Product
Do not consume any remaining sachets from the recalled lots.
Check Your Lot Numbers
Verify if your product matches one of the three recalled lot numbers: F090824LN16, F170325LN19, or 300326LN28.
Contact the Distributor
Reach out to Natur Fuel at 2725 Armstrong Avenue, Clermont, FL 34714 for further instructions on disposal or refunds.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Distributed nationwide (US).” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 30 days after the firm started it.

Sep 14, 2026Firm started the recall
Oct 7, 2026FDA classified it Class I
Oct 14, 2026Published in FDA’s Enforcement Report
Oct 21, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/1614171-a-p-creations-recalls-x10-natural-enhancement-supplement-0-5">A&amp;P Creations Recalls X10 Supplement Due to Undeclared Drugs (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #H-0016-2027 (September 14, 2026)
Plain-language summary written by qwen3.6:35b-a3b on October 21, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.