ANNOUNCED ONGOING Food recall · Reported 15 Sep 2026 · FDA company announcement, classification pending
biQ-FEL supplement recalled by A&P Creations
A&P Creations is recalling biQ-FEL supplement. The recall was initiated on 14 Sep 2026 and is listed as ongoing.
Recall details
- Recall number
- FDA-PR-8350ff324a02
- Recalling firm
- A&P Creations
- Brand
- biQ-FEL
- Classification
- Pending
- Status
- Ongoing
- Recall initiated
- 14 Sep 2026
- Reported
- 15 Sep 2026
- Reason category
- Hidden Drug Ingredients
- Product category
- Sexual Enhancement Products
Timeline
| 14 Sep 2026 | Recall initiated by company | |
| 15 Sep 2026 | Published in enforcement report | +1 day |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product contains sildenafil and tadalafil. CLERMONT, Florida - A&P Creations LLC is recalling certain lots of dietary supplement biQ-FEL 500 mL at the consumer level because it has been found to contain undeclared Sildenafil and Tadalafil. Sildenafil and Tadalafil are active ingredients in FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. As of September 14, 2026, A&P Creations LLC has not received any reports of adverse events related to this recall. The recalled product is biQ-FEL, a liquid packaged in a 500 mL bottle bearing the biQ-FEL name. The product label includes Spanish-language text, including “Sabor artificial Hierbabuena” and was distributed to consumers in the U.S. through Amazon, Walmart.com, and naturefuel.us. It includes: Lot Number Expiration Date UPC/Barcode Identifier biQ-f001-06-25 05/06/27 biQ-FEL biQ-003-01-26 01/01/28 7709799120663 A&P Creations LLC distributed biQ-FEL as a finished product and did not manufacture or formulate the product. A&P Creations LLC decided to recall biQ-FEL 500 mL after U.S. Food and Drug Administration (FDA) laboratory analysis identified sildena
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the company
biQ-FEL 500mL supplement bottle
Where it was distributed
Not stated.
Stores named: Walmart, Amazon, Online Retailers
Questions about this recall
Why was it recalled?
Product contains sildenafil and tadalafil. CLERMONT, Florida - A&P Creations LLC is recalling certain lots of dietary supplement biQ-FEL 500 mL at the consumer level because it has been found to contain undeclared Sildenafil and Tadalafil. Sildenafil and Tadalafil are active ingredients in FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. As of September 14, 2026, A&P Creations LLC has not received any reports of adverse events related to this recall. The recalled product is biQ-FEL, a liquid packaged in a 500 mL bottle bearing the biQ-FEL name. The product label includes Spanish-language text, including “Sabor artificial Hierbabuena” and was distributed to consumers in the U.S. through Amazon, Walmart.com, and naturefuel.us. It includes: Lot Number Expiration Date UPC/Barcode Identifier biQ-f001-06-25 05/06/27 biQ-FEL biQ-003-01-26 01/01/28 7709799120663 A&P Creations LLC distributed biQ-FEL as a finished product and did not manufacture or formulate the product. A&P Creations LLC decided to recall biQ-FEL 500 mL after U.S. Food and Drug Administration (FDA) laboratory analysis identified sildena
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does an unclassified recall mean?
The FDA assigns a class once it has assessed the health risk. Until then the recall is listed without one.
Read the official FDA notice · Source record retrieved 26 Sep 2026. This is a company announcement published by the FDA; the FDA has not yet classified the recall. The record is updated when the classification appears in the Enforcement Report. This page reports the record and gives no medical advice.
More recalls from A&P Creations
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | ANNOUNCED | X10 Natural Enhancement Supplement recalled by A&P CreationsX10 | A&P Creations | Hidden Drug Ingredients |
Other Sexual Enhancement Products recalls
All 9| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | ANNOUNCED | X10 Natural Enhancement Supplement recalled by A&P CreationsX10 | A&P Creations | Hidden Drug Ingredients | |
| Food | ANNOUNCED | Business Pill, Branch Manager recalled by Supplx.comBusiness Pill, Branch Manager for Men | Supplx.com | Undeclared Allergens | |
| Food | CLASS II | Pure Libido Drink recalled by Liquid Blenz | Liquid Blenz | Botulism | NY |
| Food | CLASS I | Boner Bears Honey Male Enhancement 100% Wildflower Honey recalledBoner Bears | Pure Vitamins and Natural Supplements | Undeclared Allergens | NJ |
| Food | CLASS I | Red Bull Extreme Male Enhancement Supplement recalled | Pure Vitamins and Natural Supplements | Undeclared Allergens | NJ |