MOGO PURE MORINGA OLEIFERA CAPSULES Recall: What To Do

The mogo moringa recall is a Class I action issued by the U.S. Food and Drug Administration on July 8, 2026. It affects MOGO Pure Moringa Oleifera Capsules made by MOGO Moringa LLC. The agency warns the product may be contaminated with Salmonella Typhimurium. A Class I designation is the most serious category the FDA uses. It means the product could cause serious illness or death. If you bought this supplement, this guide explains what the recall covers and what to do next.

What the Mogo Moringa Recall Covers

The mogo moringa recall covers MOGO Pure Moringa Oleifera Capsules, sold as an herbal supplement. Each bottle holds 180 quick-release veggie capsules. The label describes the product as “100% Pure.” Each capsule contains 350 mg of moringa. The supplement facts panel lists moringa powder at 1050 mg. The only listed ingredient is 100% pure moringa leaf powder from Moringa oleifera.

The product was manufactured in the USA. It was marketed by MOGO Moringa LLC, listed on the label as “MOGO Miringa LLC.” The company address is PO Box 32066, Saint L. The recall applies to a large batch of these capsules. In total, 23,186 units are affected by this action.

This recall carries FDA recall number H-1128-2026. For example, checking the recall number against your bottle can help confirm a match. However, packaging details do not always print clearly. If you own any MOGO Pure Moringa Oleifera Capsules, treat them as included until you verify otherwise. In most cases, the safest step is to assume your bottle is covered. When in doubt, follow the official notice linked below.

The Hazard and Reported Injuries

The hazard behind the mogo moringa recall is possible contamination with Salmonella Typhimurium. Salmonella is a bacteria that can cause serious foodborne illness. It spreads through contaminated food and supplements. Typically, symptoms appear within 6 hours to 6 days after exposure. Common signs include diarrhea, fever, and stomach cramps.

For most healthy adults, salmonella illness resolves on its own. However, it can be far more dangerous for some people. Young children, older adults, and those with weak immune systems face higher risk. In rare cases, the bacteria enter the bloodstream. As a result, the infection can become life-threatening and require hospital care.

The FDA record for this recall does not state whether any injuries have been reported. As a result, this guide makes no claim either way. We will not say illnesses did occur, and we will not say they did not. The Class I rating reflects the potential for serious harm, not a confirmed count of victims. The table below summarizes the verified agency details.

What To Do If You Own This Product

If you own this supplement, stop using it right away. Do not take another capsule while the mogo moringa recall is active. This is true even if the bottle looks and smells normal. Salmonella contamination is not something you can see or taste. For example, a sealed, clean-looking bottle can still carry the bacteria.

Next, identify your product carefully. Check the label for MOGO Pure Moringa Oleifera Capsules, 180 veggie capsules, 350 mg each. Compare the marketer name and address on the bottle to the recall details above. Look for the recall number H-1128-2026 in any notice you received. Keep the bottle and its packaging for now, as you may need them.

The agency record for this recall contains remedy text that does not match the product. For that reason, the remedy has been withheld here. We will not tell you what to do with the bottle beyond stopping use. Instead, follow the instructions in the official FDA notice linked on this page. In most cases, that notice explains refunds, returns, or disposal. Read the official notice here: FDA Enforcement Report

If you feel sick after taking this product, contact a doctor. Tell them you may have been exposed to salmonella. Typically, medical staff will ask about your symptoms and timeline. Keep any records of your purchase and your illness. However, seek emergency care right away if symptoms are severe.

Does a Mogo Moringa Recall Mean You Can Sue?

A recall is a safety action, not a lawsuit. The mogo moringa recall alone does not create a legal claim. It is the FDA and the company acting to remove a risky product. In most cases, a recall is meant to protect the public, not to assign blame. So owning a recalled bottle does not, by itself, mean you can sue.

A legal claim usually needs more than a recall. Typically, it requires an actual injury and a link between that injury and the product. This link is called causation. For example, a person who got sick and can tie the illness to the supplement may have a stronger footing. However, proving causation can be difficult and fact-specific.

If you believe this product harmed you, speak with a licensed attorney. A qualified lawyer can review your medical records and purchase history. They can tell you whether your situation may support a claim. You may be eligible to pursue one, but no outcome is guaranteed. This guide offers general education only, not legal advice.

How Recalls Connect to Mass Tort Cases

A recall can later become part of larger litigation. When many people are hurt by the same product, individual cases sometimes group together. This is often called a mass tort. In these situations, a recall notice can serve as important evidence. For example, it can show that a company knew about a defect and acted on it.

History shows how this can unfold. The Philips CPAP recall led to thousands of injury claims and a broad mass tort. The Takata airbag recall, one of the largest ever, also drove sweeping litigation over defective parts. However, those cases involved confirmed, widespread harm and years of court work. A recall like this one is only a first step. As a result, it may or may not ever lead to any lawsuit at all.

Frequently Asked Questions

What products are part of the mogo moringa recall?

The recall covers MOGO Pure Moringa Oleifera Capsules, 180 veggie capsules per bottle, 350 mg each. It was issued by the FDA under recall number H-1128-2026. In total, 23,186 units are affected.

Why were these moringa capsules recalled?

The product may be contaminated with Salmonella Typhimurium. That bacteria can cause serious illness, especially in vulnerable people. The FDA classified it as Class I, its most serious level.

Can I get a refund or return the product?

The remedy details in the agency record did not match this product, so they were withheld here. Do not rely on any remedy claim from this page. Instead, follow the instructions in the official FDA notice linked above.

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 July 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.