FDA Food recall ·
MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- H-1128-2026
- Date
- (initiated May 24, 2026)
- Company / brand
- MOGO Moringa LLC
10443 Corbeil Dr, Saint Louis, MO, United States - Category
- Food › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 23,186 bottles
- Hazard tags
- Salmonella Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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
Why was it recalled?
Product may be contaminated with Salmonella Typhimurium
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028
Distribution
Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (food), recall H-1128-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.