RecallRadar
FDA · FoodClass I

A&p Creations food recall: X10 Natural Enhancement Supplement

Undeclared allergens

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
99872
Recall initiated
Sep 14, 2026
Classified by FDA
Oct 7, 2026
Posted in Enforcement Report
Oct 14, 2026
Recalling firm
A&P CREATIONS
Firm location
Clermont, FL, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Press Release
Products in this event
2

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Product contains undeclared Sildenafil and Tadalafil.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Sep 14, 2026. FDA classified it 23 days later, on Oct 7, 2026. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: Distributed nationwide (US).

Recalled products (2)

  • H-0016-2027 Class I Ongoing

    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.

    Codes / lots: Lot # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.

    Quantity: 1,283 retail units

  • H-0017-2027 Class I Ongoing

    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

    Codes / lots: Lot # biQ-f001-06-25, Expiry: 05/06/2027; Lot # biQ-003-01-26, Expiry: 01/01/28

    Quantity: 3,116 bottles

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 99872
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.