Home › Over-the-counter & supplements › A&P Creations LLC Issues Nationwide Recall of…
A&P Creations LLC Issues Nationwide Recall of biQ-FEL
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
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…
The Recall Registry rates this highest risk — Contains a drug ingredient that is not on the label.
What to do
Read the full announcement on FDA.gov using the link below — it lists the affected lots and what the company is offering.
Who to contact: Announced by A&P Creations LLC
Details
- Recall date
- September 14, 2026
- Brand
- A&P Creations LLC
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 LLC Issues Nationwide Recall of biQ-FEL Due to Undeclared Sildenafil and Tadalafil”
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