Class IOngoingVoluntary: Firm initiated
MOGO Moringa LLC: food recall H-1128-2026
MOGO Moringa LLC of Saint Louis, MO recalled MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER… Reason: Product may be contaminated with Salmonella Typhimurium. The FDA listed it as Class I in its Enforcement Report dated Jul 8, 2026; distribution: nationwide.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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 by: MOGO MIRINGA LLC, PO BOX 32066 Saint Louis, MO 63132
- Product quantity
- 23,186 bottles
- Reason for recall
- Product may be contaminated with Salmonella Typhimurium
- Codes, lots and dates on the package
- Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028
- Distribution pattern
- Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)
- Recalling firm
- MOGO Moringa LLC, Saint Louis, MO
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 24, 2026 |
| Classified by the FDA | Jun 29, 2026 |
| Published in the Enforcement Report | Jul 8, 2026 |
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OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1128-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.