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CLASS I · SeriousFDA

A&P CREATIONS recalls biQ-FEL

📅 Sep 14, 2026 · 📍 Nationwide
Recalling company
A&P CREATIONS
Product
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
Reason
Product contains undeclared Sildenafil and Tadalafil.
Classification
Class I – a reasonable probability that use will cause serious adverse health consequences or death
Recall date
Sep 14, 2026
Reported
Oct 14, 2026
Distribution
Distributed nationwide (US).
Status
Ongoing
Quantity
3,116 bottles
Lot / codes
Lot # biQ-f001-06-25, Expiry: 05/06/2027; Lot # biQ-003-01-26, Expiry: 01/01/28
Company location
Clermont, FL
Recall type
Voluntary: Firm initiated
Recall number
H-0017-2027
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number H-0017-2027 in the FDA Enforcement Report. Also see FDA recall press releases.

⚠️ If you have this product, don’t eat or use it. Return it to the store or throw it away, and follow the instructions in the official notice. If you feel sick, contact your healthcare provider. FoodRecallNow summarizes public data and is not affiliated with the FDA.