Food recall

A&P CREATIONS recall: X10 Natural Enhancement Supplement

A&P CREATIONS, of Clermont, FL, recalled X10 Natural Enhancement Supplement and 1 other product. The FDA's reason: “Product contains undeclared Sildenafil and Tadalafil.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on September 14, 2026, and the FDA first listed it in its Enforcement Report of October 14, 2026. The recall is still going on.

How serious

Class I

It could cause serious harm or death

Why

Other ingredient not on the label (sulfites, dyes...)

Status

Ongoing

The recall

Company
A&P CREATIONS (Clermont, FL)
Reason, in FDA's words
“Product contains undeclared Sildenafil and Tadalafil.”
Where it was sold
Distributed nationwide (US).
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
99872

The 2 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0016-2027 Class I

    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: 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

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

    Quantity: 3,116 bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of October 14, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.