Recall Summary
| Recall number | H-1196-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-08-12 |
| Company | AKKARCO LLC |
| Units affected | 1,052 |
| 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 akkarco ashfiat recall is a Class I action announced by the U.S. Food and Drug Administration. AKKARCO LLC recalled Ashfiat Alharamain Energy Support 250ml/8fl. oz. The reason is undeclared tadalafil. That is a prescription drug ingredient not listed on the label. The FDA assigned recall number H-1196-2026 on August 12, 2026.
About 1,052 units are affected. Class I is the FDA’s most serious category. It means there is a reasonable probability that use will cause serious health problems or death. If you bought this product, this guide explains what the record says.
What the Akkarco Ashfiat Recall Covers
The akkarco ashfiat recall covers one product. It is Ashfiat Alharamain Energy Support, sold in a 250ml bottle. That is eight fluid ounces. The recalling firm is AKKARCO LLC. The FDA is the issuing agency. The recall number is H-1196-2026.
The scope is 1,052 units. That is a relatively small distribution. However, small volume does not mean low risk. The Class I severity rating is driven by the hazard, not the count. For example, a single bottle containing an undeclared prescription drug can harm one person seriously.
Products like this are typically marketed as energy or wellness supplements. In most cases they are sold as dietary supplements rather than drugs. As a result, buyers often assume the ingredient list is complete. That assumption is what makes undeclared active ingredients dangerous.
The FDA record does not publish additional lot codes or date ranges on the summary entry. It also does not list every retail location in the public summary. If you need lot-level detail, check the official notice linked on this page. That notice is the controlling document for identification.
The Hazard and Reported Injuries
The hazard in the akkarco ashfiat recall is undeclared tadalafil. Tadalafil is a prescription medicine. It is the active ingredient in drugs used for erectile dysfunction and certain blood pressure conditions. It is not permitted as a hidden ingredient in a supplement.
Tadalafil lowers blood pressure. That effect is the core concern here. It can interact dangerously with nitrates. Nitrates are commonly prescribed for heart disease and chest pain. As a result, a person taking nitrates who consumes hidden tadalafil may experience a sudden drop in blood pressure.
Typically, people who use energy supplements do not know they are taking a prescription drug. They cannot warn their doctor. They cannot check for interactions. However, that is exactly the population most at risk. Men with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates.
The FDA record does not state whether injuries have been reported in connection with this recall. This guide does not claim that injuries occurred. It also does not claim that none occurred. The public record simply does not address the question.
| Recall number | H-1196-2026 |
|---|---|
| Issuing agency | U.S. Food and Drug Administration |
| Recall date | August 12, 2026 |
| Company | AKKARCO LLC |
| Product | Ashfiat Alharamain Energy Support 250ml/8fl. oz. |
| Hazard | Undeclared tadalafil |
| Units affected | 1,052 |
| Severity classification | Class I |
What To Do If You Own This Product
Stop using the product first. Do not finish the bottle. Do not give it away or resell it. That is the standard first step for any Class I recall. The akkarco ashfiat recall is no exception.
Next, identify what you have. Look at the label for the name Ashfiat Alharamain Energy Support. Check the size, which is 250ml or 8 fluid ounces. Check for AKKARCO LLC on the packaging. Photograph the label and the bottle before you do anything else.
Do not follow secondhand instructions about refunds or returns. The remedy details in the public agency entry for this recall do not match the product. For that reason, this guide does not state what the remedy is. Instead, follow the instructions in the official FDA notice linked on this page: FDA Enforcement Report — recall H-1196-2026
Talk to a doctor if you used the product. This matters most if you take nitrates or heart medication. Mention the undeclared tadalafil specifically. However, do not stop any prescribed medication on your own. You can also report a problem to the FDA through MedWatch. Keep your receipt and the product if you can do so safely.
Does a Akkarco Ashfiat Recall Mean You Can Sue?
No. A recall is not a lawsuit. This is the single most misunderstood point in consumer safety news. A recall is a regulatory and safety action. It removes a product from the market. It does not decide who is legally responsible for anything.
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The akkarco ashfiat recall tells you the FDA classified a hazard. It does not tell you that anyone has a legal claim. In most cases, a product liability claim needs more than a recall notice. It typically needs an actual injury. It also needs causation, meaning a link between the product and that injury.
For example, buying a recalled bottle and never using it usually does not create a personal injury claim. Using it and suffering a documented medical event is a different situation. That is where a claim may exist. However, that determination depends on medical records, timing, and state law.
If you believe you were harmed, speak with a licensed attorney in your state. Bring your medical records and any remaining product. You may be eligible to pursue a claim. No one can promise an outcome, and this guide does not. Deadlines called statutes of limitation also apply and vary by state.
How Recalls Connect to Mass Tort Cases
Recalls often show up later as evidence. They do not create liability by themselves. However, they document what a company knew and when. A recall notice can establish a timeline. As a result, plaintiffs’ lawyers frequently use recall records as an anchor in later litigation.
Two real examples show the pattern. Philips recalled millions of CPAP and ventilator devices in 2021 over degrading sound abatement foam. Thousands of injury claims followed and were consolidated into multidistrict litigation. Takata airbag inflators were recalled across many automakers, and that recall record fed years of injury and economic loss litigation. In both cases, the recall came first and the litigation came later, built on separate proof of injury and causation.
Frequently Asked Questions
What does Class I mean in the akkarco ashfiat recall?
Class I is the FDA’s most serious recall classification. It means there is a reasonable probability that using the product will cause serious health consequences or death. It reflects the severity of the hazard, not how many units were sold.
Why is undeclared tadalafil dangerous?
Tadalafil is a prescription drug that lowers blood pressure. When it is hidden in a supplement, consumers cannot tell their doctor or check for interactions. It can be especially risky for people taking nitrates for heart conditions.
Were any injuries reported in this recall?
The FDA record for recall H-1196-2026 does not state whether injuries were reported. This guide will not claim injuries occurred or that none occurred. Check the official notice for any updates.
How do I get a refund or return the product?
Follow the instructions in the official FDA notice linked on this page. The remedy language in the public summary does not match this product, so it is not repeated here. Contact AKKARCO LLC through the details in that notice.
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 August 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.