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ACTIVE RECALL — CLASS IActive recallH-0017-2027/FDA enforcement
A&p Creations·Food·Sep 14, 2026

Biq-fel, 16.9 FL OZ (500 ML), 17 Servings Per Bottle, Manufactured by Almenat Sas Av 39 Oeste…

What you need to know

Class I

  • What happened

    Product contains undeclared Sildenafil and Tadalafil.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A prescription drug ingredient hidden in a product sold as a supplement or food, creating serious cardiac risks.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Active recall · classified by the FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameA&p Creations
Recalling firmA&p CreationsClermont, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot # biQ-f001-06-25, Expiry: 05/06/2027
  • Lot # biQ-003-01-26, Expiry: 01/01/28
Distribution area
Nationwide

Distributed nationwide (US).

United States

Quantity affected3, 116 bottles
Recall initiationFDA report date: October 14, 2026
FDA recall numberH-0017-2027

Beyond the headline

The recall, in context

A&p Creations initiated this food recall on September 14, 2026. The FDA enforcement report states: Product contains undeclared Sildenafil and Tadalafil. The FDA report lists distribution as: Distributed nationwide (US).

The FDA enforcement report describes the reason as: Product contains undeclared Sildenafil and Tadalafil.

Biq-fel, 16.9 FL OZ (500 ML), 17 Servings Per Bottle, Manufactured by Almenat Sas Av 39 Oeste… was made or distributed by A&p Creations in Clermont, FL, United States. This page reflects FDA report H-0017-2027, dated October 14, 2026.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a prescription drug ingredient hidden in a product sold as a supplement or food, creating serious cardiac risks.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Biq-fel, 16.9 FL OZ (500 ML), 17 Servings Per Bottle, Manufactured by Almenat Sas Av 39 Oeste… recall?

A&p Creations recalled Biq-fel, 16.9 FL OZ (500 ML), 17 Servings Per Bottle, Manufactured by Almenat Sas Av 39 Oeste… in an FDA Class I enforcement action reported as H-0017-2027. Product contains undeclared Sildenafil and Tadalafil.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

Is the A&p Creations recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0017-2027. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.