MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT
Recalled by MOGO Moringa LLC
Food recall
MOGO Moringa LLC
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
MOGO Moringa LLC has recalled MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on July 8, 2026 and was initiated on May 24, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, with approximately 23,186 bottles affected. The company behind the recall is MOGO Moringa LLC, based in Saint Louis, MO. The FDA describes the product as: “MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE, SUPPLEMENT FACTS MORINGA POWDER 1050 mg, Ingredients: 100% Pure Moringa Leaf Powder (Moringa Oleifera), MANUFACTURED IN USA AND Marketed b…”
Why was MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT recalled?
According to the FDA, the stated reason for the recall is: “Product may be contaminated with Salmonella Typhimurium.” In plain terms, this recall relates to Salmonella.
Salmonella is a group of bacteria that is one of the most common causes of foodborne illness in the United States. Public health authorities note that infections can lead to symptoms such as fever, diarrhea, and stomach cramps, and that young children, older adults, and people with weakened immune systems are at higher risk of serious illness. Because it can spread through contaminated food, regulators treat Salmonella findings seriously.
What should you do?
If you think you may have bought MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, compare it against the product description and identifying codes (Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact MOGO Moringa LLC or your local health authority.
About this recall
This recall was distributed in MO. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- July 8, 2026
- Recall started
- May 24, 2026
- Distributed in
- MO
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT recalled?+
According to the FDA: Product may be contaminated with Salmonella Typhimurium
How serious is this recall?+
Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.
What should I do if I have MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-1128-2026. Information last synced from the FDA on July 14, 2026.
