FDA recall, , High risk
Mogo Pure Moringa Oleifera Capsules
Moringa capsules may be contaminated with Salmonella Typhimurium.
Summary by Recall Canary from the FDA notice
What happened
Mogo Moringa LLC, based in Saint Louis, Missouri, is voluntarily recalling specific lots of its Mogo Pure Moringa Oleifera Capsules, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE, because the product may be contaminated with Salmonella Typhimurium. The company began the recall on May 24, 2026, and announced it on May 25, 2026.
The recalled capsules were sold nationwide via ecommerce, including Amazon, Ebay, Etsy, and mogomiranga.com. The product is manufactured in the USA and marketed by MOGO MIRINGA LLC, PO BOX 32066 Saint Louis, MO 63132. The recall covers 23,186 bottles.
What to do
If a code on your package is listed below:
- You may also contact Mogo Moringa LLC directly using the contact information provided on the recall page.
- Consumers who have product from the affected lots are recommended not to use the product.
- For complete information, including guidance and support related to this recall, consumers are encouraged to visit the company’s official recall information page. Https://www.mogomoringa.com/pages/product-recall-submission-form.
Is yours affected?
Match the lot code and expiration date listed under your product.
Mogo Pure Moringa Oleifera Capsules
- Lot code
- 15525AA
- 00926AA
- Expiration date
- 06/2027, 01/2028
Recall details
- Company began the recall
- Sold in
Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)
- Company
- MOGO Moringa LLCSaint Louis, Missouri
- Hazard
- Salmonella
- Risk
High risk
There is a reasonable chance that taking it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 99071
- Recall number
- H-1128-2026
- Quantity recalled
- 23,186 bottles
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Announced by the company
Listed on Recall Canary
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Summary updated
