Class I — Most Severe

biQ-FEL Supplement Recalled for Undeclared Ingredients

FreshRecall Team A&P Creations LLC Undeclared Drug
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Class I Recall — Most Serious

This is a Class I recall — the most serious type. Products covered by this recall may cause serious health consequences or death.

Front of bottle, biQ-FEL 500mL Back of bottle, biQ-FEL 500mL

A&P Creations LLC has announced a nationwide recall of its biQ-FEL dietary supplement due to the presence of undeclared Sildenafil and Tadalafil. These ingredients are typically found in prescription medications used to treat erectile dysfunction and can pose serious health risks if taken without medical supervision.

Products Affected:

  • biQ-FEL 500 mL supplement bottles
  • Lot Numbers: biQ-f001-06-25 (Exp. 05/06/27) and biQ-003-01-26 (Exp. 01/01/28)
  • UPC: 7709799120663

The product was distributed through Amazon, Walmart.com, and naturefuel.us, and features Spanish-language labeling including “Sabor artificial Hierbabuena.”

Reason for Recall:

The recall was initiated after FDA laboratory analysis revealed the presence of Sildenafil and Tadalafil, which were not listed on the product label. These ingredients can dangerously lower blood pressure, especially in individuals taking nitrates for conditions such as diabetes, high blood pressure, high cholesterol, or heart disease.

Consumer Action:

Consumers are advised to stop using the recalled product immediately and destroy it. For questions, contact A&P Creations LLC at [email protected], Monday to Friday, 9:00 am to 4:00 pm ET. If you have experienced any health issues related to this product, consult your healthcare provider.

No adverse events have been reported to date. However, any reactions or quality issues can be reported to the FDA's MedWatch Adverse Event Reporting Program online.

This recall is conducted with the knowledge of the U.S. Food and Drug Administration.

Affected Products

Product Name UPC Lot Number Expiration Date
biQ-FEL 500mL supplement bottle biQ-FEL biQ-f001-06-25 05/06/27
biQ-FEL 500mL supplement bottle 7709799120663 biQ-003-01-26 01/01/28

Where Products Were Sold

This recall affects products distributed nationwide across the United States.

Contact Information

Consumer Contact

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View original FDA announcement