FDAFDA recall H-0016-2027 · Oct 14, 2026
A&P CREATIONS: X10 Natural Enhancement Supplement recall
Recall found
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.
Reason for recall
Product contains undeclared Sildenafil and Tadalafil.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- Lot # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.
- Quantity
- 1,283 retail units
- Distribution
- Distributed nationwide (US).
- Recalling firm
- A&P CREATIONS, Clermont, FL
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-09-14
Source: openFDA enforcement record H-0016-2027 · search recall number H-0016-2027 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 21, 2026, 12:30 AM EDT. The agency notice is the final word.