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H-0017-2027Class I

A&P CREATIONS

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
A&P CREATIONS
Product type
Food / supplement / cosmetic
Status
Ongoing
Report date
2026-10-14
Distribution
Distributed nationwide (US).
Firm state
FL
Product quantity
3,116 bottles
Initiated by
Voluntary: Firm initiated
Reason for recall

Product contains undeclared Sildenafil and Tadalafil.

Product description

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

Code / lot info

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

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →