Byron White FORMULAS A-FNG Herbal Supplement
Reason Label does not declare walnuts in English
Mogo Pure Moringa Oleifera Capsules recall
Recalled by MOGO Moringa LLC · Saint Louis, MO, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may be contaminated with Salmonella Typhimurium
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
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
Quantity: 23,186 bottles
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028
Where it was sold
Nationwide.
FDA's distribution note: Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall.
- Recalling firm
- MOGO Moringa LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 24, 2026
- In FDA report of
- Jul 8, 2026
- FDA recall number
- H-1128-2026 · event 99071
- Official record
- FDA enforcement report search
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