MOGO Moringa LLC food recall: Mogo Pure Moringa Oleifera Capsules
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 99071
- Recall initiated
- May 24, 2026
- Classified by FDA
- Jun 29, 2026
- Posted in Enforcement Report
- Jul 8, 2026
- Recalling firm
- MOGO Moringa LLC
- Firm location
- Saint Louis, MO, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Product may be contaminated with Salmonella Typhimurium
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on May 24, 2026. FDA classified it 36 days later, on Jun 29, 2026. Distribution reported by FDA: Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)
Recalled products (1)
H-1128-2026 Class I Ongoing
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
Codes / lots: Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028
Quantity: 23,186 bottles
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 99071
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.