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A&P CREATIONS — biQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle
Stop taking it and tell your doctor or pharmacist.
Why this is on The Recall Registry: This is a consumable product recalled for what is inside it. It was found to contain a drug or chemical that is not on the label. That is different from an allergen or a contamination scare: anyone taking it has been taking a substance nobody prescribed, in an unknown dose, and it can interact with medication they are already on. Follow the agency notice rather than judging it by how the product looks.
What’s wrong
Product contains undeclared Sildenafil and Tadalafil.
The Recall Registry rates this highest risk — FDA Class I: reasonable probability of serious harm or death.
What to do
Stop taking it, and tell your doctor or pharmacist that you have been taking it. It contains a drug ingredient that is not on the label, so they need to know — it can interact with medication you are already on.
Who to contact: Recalling firm: A&P CREATIONS
The 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
Details
- Units affected
- 3,116 bottles
- Recall date
- September 14, 2026
- Brand
- A&P CREATIONS
Distributed nationwide (US)
The official notice
This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.
Their exact wording: “A&P CREATIONS — 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”
Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.
Filed under: Over-the-counter & supplements