RecallHawk
Class I Recall

MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE,

MOGO Moringa LLC

Summary

The FDA issued a Class I for MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE by MOGO Moringa LLC. Reason: Product may be contaminated with Salmonella Typhimurium.

Details

Source

Food Recall

External ID

H-1128-2026

Action Date

2026-07-08

Status

Ongoing

Category

food

Product Description

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

Lot/Code Info: Lot codes: 15525AA exp date: 6/2027 00926AA exp date: 1/2028

Quantity Affected: 23,186 bottles

Reason for Recall

Product may be contaminated with Salmonella Typhimurium

Distribution

Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)

Type: Voluntary: Firm initiated

Recall Initiated: 2026-05-24

Company

MOGO Moringa LLC

Saint Louis, MO

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 54 food recalls issued in the same week, part of 101 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (MOGO Moringa LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does MOGO Moringa LLC have FDA actions?

This is the only FDA action we have on record for MOGO Moringa LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1128-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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