Zen Principle Naturals Moringa Leaf Powder dietary Recall: What To Do

factory6 zen recall notices are now circulating for a widely sold herbal supplement. On August 12, 2026, the U.S. Food and Drug Administration recorded a Class I recall by FACTORY6, INC. The action covers Zen Principle Naturals Moringa Leaf Powder capsules. The reason listed is possible Salmonella contamination in the moringa leaf powder.

Class I is the FDA’s most serious category. It means the agency believes exposure could cause serious health problems or death. If a bottle of this supplement sits in your cabinet, this guide explains what the record says.

What the Factory6 Zen Recall Covers

The factory6 zen recall applies to one specific dietary supplement product. It is Zen Principle Naturals Moringa Leaf Powder in capsule form. Each capsule contains 900mg. Each bottle holds 180 capsules. The bottles are white PET plastic. The labeled directions call for two capsules per day. The route of administration is oral. The product is offered as a 1-pack containing 180 capsules.

The label points to Zen Principle at 774 Mays Blvd, Incline Village, NV 89451. That is the “manufactured for” address on the bottle. The recalling firm of record is FACTORY6, INC. Shoppers often recognize the Zen Principle Naturals brand name rather than the corporate one. For example, a buyer may not connect the recall headline to the bottle on the shelf. Check the front label carefully.

The FDA assigned this action recall number H-1222-2026. The recall event date in the record is August 12, 2026. The scope listed is 2,048 units. That is a modest quantity by supplement standards. However, unit counts do not measure risk. A Class I designation reflects the seriousness of the hazard, not the size of the batch.

The agency record does not spell out every retail channel in the data summarized here. Moringa supplements typically sell through online marketplaces and health retailers. In most cases, buyers should check order history and email receipts. Do not assume you are unaffected because you bought online. The official notice linked on this page is the authoritative source for distribution details.

The Hazard and Reported Injuries

The stated hazard is possible Salmonella in the moringa leaf powder. Salmonella is a bacterium that causes salmonellosis. Typical symptoms include diarrhea, fever, abdominal cramps, nausea, and vomiting. Symptoms usually begin within six hours to six days after exposure. Most healthy adults recover within about a week without hospital care.

However, some people face far greater risk. Young children, older adults, pregnant people, and those with weakened immune systems are more vulnerable. In those groups, the infection can move from the intestines into the bloodstream. As a result, it can reach bones, joints, or the nervous system. Those invasive infections can require hospitalization and can be fatal.

Supplements carry a particular concern. They are often taken daily and for long stretches. This label directs two capsules per day, every day. As a result, exposure may be repeated rather than one-time. People also take supplements for health reasons, which means some users may already be medically fragile.

Whether any injuries or illnesses have been reported in connection with this recall is not stated in the agency record reviewed here. This guide will not claim illnesses occurred, and it will not claim none did. Readers who feel unwell should speak to a clinician rather than rely on a recall notice. Below is the verified record at a glance.

What To Do If You Own This Product

Stop taking the capsules first. Do not finish the bottle to avoid waste. A Class I hazard is not a reason to use up remaining product. Set the bottle aside where nobody else will grab it. Keep it away from children and household pets.

Next, identify what you have. Look for the Zen Principle Naturals name on the front of the bottle. Confirm the product is Moringa Leaf Powder in 900mg capsules. Confirm the count is 180 capsules. Check for the white PET bottle described in the record. Photograph the front and back labels before you do anything else.

The remedy instructions in the agency record could not be confirmed as matching this product, so this guide does not state them. Follow the instructions in the official notice linked on this page instead. That notice controls. For example, it will explain how to handle the bottle and who to contact. Do not rely on secondhand social media posts describing the process.

Keep documentation either way. Save your receipt, order confirmation, or credit card statement. Keep the bottle and its label unless the official notice directs otherwise. Typically, records like these matter later far more than people expect. If you developed symptoms, seek medical care and keep those records too. You can also report a problem to FDA MedWatch.

Does a Factory6 Zen Recall Mean You Can Sue?

A recall is a safety action. It is not a lawsuit. The factory6 zen recall is a regulatory event recorded by the FDA. It removes product from the market and warns the public. It does not by itself create a legal claim for anyone. That distinction matters and is often misunderstood.

In most cases, a personal injury claim needs more than a recall notice. It typically needs an actual injury. It also needs causation, meaning a link between the product and the harm. Proof of purchase and use is usually required as well. Medical records, lab results, and the product itself can all matter. Without those elements, a recall alone is not a claim.

For example, someone who bought the supplement but never opened the bottle generally has no injury claim. Someone who became seriously ill after taking it may have a different situation. However, illness alone does not prove the supplement caused it. Salmonella has many possible sources, including other foods. Causation is a factual question that requires evidence.

Nobody here can tell you whether you have a case. If you believe you were harmed, talk to a licensed attorney in your state. Many offer free consultations for product cases. You may be eligible to pursue a claim, depending on your facts. There are no guarantees of any recovery, and deadlines called statutes of limitations can apply.

How Recalls Connect to Mass Tort Cases

Recalls and mass torts are separate things that sometimes intersect. A recall is the regulatory record of a defect or contamination. Litigation, when it happens, comes later and is driven by injured people. However, a recall can become important evidence in that litigation. It can help establish what a company knew and when it acted.

History shows the pattern. Philips recalled millions of CPAP and BiPAP devices in 2021 over degrading sound abatement foam. Thousands of injury claims followed and were consolidated into multidistrict litigation. Takata’s airbag inflator recalls became one of the largest automotive recalls ever, and extensive litigation followed. In both cases, the recall documentation was a starting point, not the claim itself.

Food and supplement contamination cases follow similar logic. Plaintiffs typically must tie a specific illness to a specific contaminated product. As a result, laboratory confirmation of the pathogen is often central. Nothing in this guide asserts that litigation exists over the factory6 zen recall. No lawsuit connected to this recall has been verified here.

Frequently Asked Questions

What product is covered by the factory6 zen recall?

It covers Zen Principle Naturals Moringa Leaf Powder dietary supplement capsules. The capsules are 900mg, packaged 180 per white PET bottle, sold as a 1-pack. The recalling firm is FACTORY6, INC., under FDA recall number H-1222-2026.

Why is the factory6 zen recall classified as Class I?

Class I is the FDA’s most serious recall class. It is used when there is a reasonable probability that use of the product could cause serious health consequences or death. Here, the hazard listed is possible Salmonella in the moringa leaf powder.

How do I get the remedy for the factory6 zen recall?

Follow the instructions in the official FDA notice linked on this page. That notice is the authoritative source for how affected buyers should proceed. This guide does not state the remedy because the remedy text in the agency record did not match this product.

Should I see a doctor after taking this supplement?

If you have symptoms such as fever, diarrhea, vomiting, or cramps, contact a clinician. Tell them you took a supplement subject to a Salmonella-related recall. People at higher risk, including young children and older adults, should not wait to seek care.

Does the factory6 zen recall mean I automatically get money?

No. A recall is a safety action, not a payout and not a lawsuit. Depending on your injury and evidence, you may be eligible to pursue a claim, but that requires a licensed attorney’s review of your specific facts.

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.

Related Guides

• All Product Recalls
• All Active MDL Cases
• Mass Tort Explainers
• Mass Tort Tips
• Tort Reform by State — 50-State Comparison

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.