Recall Summary
| Recall number | H-0017-2027 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-10-14 |
| Company | A&P CREATIONS |
| Units affected | 3,116 |
| Severity | Class I |
Remedy: Follow the instructions in the official notice linked below. The agency record for this recall did not contain remedy text we could verify against this product, so we have not reproduced it here.
Read the official U.S. Food and Drug Administration recall notice
The creations biq-fel recall involves a liquid product called biQ-FEL. A&P CREATIONS recalled 3,116 units after a serious problem came to light. The U.S. Food and Drug Administration reports that the product contains undeclared sildenafil and tadalafil. These are prescription drug ingredients that were not listed on the label. As a result, people could take them without knowing it. That matters most for anyone who takes heart medicine or other prescription drugs.
What the Creations Biq-Fel Recall Covers
The recall covers biQ-FEL sold in a 16.9 fl oz (500 mL) bottle. Each bottle holds 17 servings, according to the agency record. The label states the product was manufactured by ALMENAT SAS. The listed address is AV 39 OESTE No 10 OESTE-18 CALI VALLE, and the label also reads INDUSTRIA COLOMBIANA. Biofel is listed as the distributor.
The FDA lists the recalling firm as A&P CREATIONS. The agency logged the recall under number H-0017-2027. The record is dated October 14, 2026. In total, 3,116 units fall under the creations biq-fel recall. The FDA placed it in its most serious recall category.
The agency data we reviewed does not list lot codes or expiration dates. It also does not say which stores or websites sold the product. However, that does not mean any bottle is safe to use. Typically, a recall like this applies to all units described in the notice. Check the official FDA notice for any lot or distribution details.
If you bought biQ-FEL, compare your bottle to the description above. Look for the 500 mL size and the 17-serving count. Then check for the ALMENAT SAS manufacturer line. For example, the distributor name Biofel should also appear on the label. If those details match, treat your bottle as part of the creations biq-fel recall.
The Hazard and Reported Injuries
The core problem is simple. The product contains sildenafil and tadalafil, but the label does not say so. Sildenafil is the active ingredient in Viagra. Tadalafil is the active ingredient in Cialis. Both are prescription drugs used to treat erectile dysfunction. In the United States, people need a doctor’s prescription to get them.
These drugs belong to a class called PDE-5 inhibitors. They can interact with nitrates found in some prescription heart medicines. Nitroglycerin is one common example. Taken together, the combination may lower blood pressure to dangerous levels. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. As a result, they may face the greatest risk from a hidden dose.
The FDA rated the creations biq-fel recall as Class I. This is the most serious category the agency uses. Class I means there is a reasonable probability of serious health problems or death. However, the label describes potential risk. It is not a finding that anyone was harmed.
The agency record does not state whether any injuries have been reported. We make no claim either way. If you had a reaction after drinking biQ-FEL, talk to a doctor. You can also report the reaction to the FDA. The key recall details are listed below.
| Detail | Information |
|---|---|
| Recall number | H-0017-2027 |
| Agency | U.S. Food and Drug Administration |
| Date | October 14, 2026 |
| Company | A&P CREATIONS |
| Product | biQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle |
| Hazard | Undeclared sildenafil and tadalafil |
| Units affected | 3,116 units |
| Severity | Class I |
What To Do If You Own This Product
If you have a bottle covered by the creations biq-fel recall, stop using it right away. Do not give it to anyone else. Store it away from children and pets. In most cases, keep the bottle for now instead of throwing it out. It can serve as a record if questions come up later.
Next, confirm that your product matches the recall. Check the bottle size, serving count, manufacturer, and distributor lines. Take clear photos of the front label, back label, and any printed codes. Save your receipt, order confirmation, or bank statement showing the purchase. These records show what you bought and when.
We have not listed the remedy for this recall here. The agency record we received contained remedy text that did not match this product. As a result, we withheld it rather than risk giving you wrong instructions. Please follow the steps in the official notice linked below. It is the best source for return, refund, or disposal guidance:
Official FDA recall notice for biQ-FEL
Talk to your doctor if you drank this product, especially if you take nitrates. Tell them it may contain sildenafil and tadalafil. Seek emergency care if you feel faint, very dizzy, or have chest pain. You can report side effects through FDA MedWatch. These reports help the agency track safety problems with products like this one.
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Does a Creations Biq-Fel Recall Mean You Can Sue?
A recall is not a lawsuit. It is a safety action meant to get a risky product off the market. The creations biq-fel recall warns consumers about a hazard. However, it does not decide who is legally responsible for any harm. It also does not create a legal claim on its own.
We have not verified any lawsuit filed over this recall. Owning a recalled bottle is typically not enough for a personal injury claim. In most cases, a claim needs two things. First, you need an actual injury. Second, you need evidence that the product caused that injury.
For example, say someone drank biQ-FEL and later had a serious drop in blood pressure. Their medical records would matter. So would proof of purchase and the product itself. The timing between use and symptoms would matter too. An attorney would weigh all of these facts together.
If you believe you were harmed, speak with a licensed attorney in your state. Many offer free consultations. Filing deadlines called statutes of limitations apply, so do not wait too long. Depending on your facts, you may be eligible to pursue a claim. However, no outcome is guaranteed, and every case is different.
How Recalls Connect to Mass Tort Cases
A recall can become evidence in later litigation. Recall notices, agency records, and company statements may show when a problem was known. Lawyers often use them to build a timeline. However, a recall alone does not prove that a company is liable. Courts still require proof of injury and causation.
The Philips CPAP recall is one well-known example. In 2021, Philips recalled millions of sleep apnea devices over breakdown of their sound-dampening foam. Lawsuits followed, and federal cases were consolidated in Pennsylvania. Takata airbags offer another example. Defective inflators led to the largest auto recall in U.S. history. Lawsuits and government action followed for years.
Not every recall leads to a mass tort. In fact, most never do. Typically, mass torts form when many people report similar injuries from the same product. Nobody knows yet whether the creations biq-fel recall will ever lead to lawsuits. For now, it remains a safety action.
Frequently Asked Questions
What is the creations biq-fel recall?
It is an FDA Class I recall of biQ-FEL by A&P CREATIONS, dated October 14, 2026. The product contains undeclared sildenafil and tadalafil. It covers 3,116 units of the 16.9 fl oz bottle.
Is it dangerous to drink biQ-FEL?
The hidden drugs can interact with nitrates and may lower blood pressure to dangerous levels. People with heart conditions may face higher risk. Stop using the product and talk to a doctor if you have concerns.
How do I return the product or get a refund?
We withheld the remedy because the agency text did not match this product. Follow the instructions in the official FDA notice linked on this page. That notice is the most reliable source for the creations biq-fel recall.
Were You Injured by a Recalled Product?
A recall by itself is a safety action, not a legal claim. However, if a recalled product caused a real injury, you may be eligible to pursue compensation. A licensed attorney can review your situation at no upfront cost — most work on contingency, meaning you pay nothing unless you recover.
Official Sources & Resources
Verify every recall against the issuing agency before acting:
- U.S. Food and Drug Administration: official recall database — the record of truth for this notice
- CPSC: cpsc.gov — household goods, toys, furniture, appliances
- FDA: fda.gov — food, drugs, and medical devices
- NHTSA: nhtsa.gov — vehicles, tires, and child car seats
- USDA FSIS: fsis.usda.gov — meat, poultry, and egg products
Content last reviewed October 2026. This is general educational information, not legal advice. If you notice outdated information, please contact us.
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Attorney Advertising. The information on this page is provided for general informational purposes only and does not constitute legal advice. A product recall is a safety action by a manufacturer or regulator and does not by itself establish liability or create a legal claim. No attorney-client relationship is created by accessing or using this content. Every case is unique. If you believe you were harmed by a recalled product, consult a licensed attorney in your jurisdiction.