MOGO Moringa LLC Recall: Product may be contaminated with Salmonella Typhimurium

🇺🇸 United States

1. May 24, 2026 - Recall initiated
2. July 8, 2026 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-1128-2026

Event ID

99071

Status

Ongoing

Classification

Class I

Company

MOGO Moringa LLC

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

Quantity

23,186 bottles

Reason

Product may be contaminated with Salmonella Typhimurium

Recall initiation date

May 24, 2026

Report date

July 8, 2026

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

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

UPC, lot, and code information

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

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Linked outbreak investigation

This recall has been explicitly confirmed as connected to the outbreak investigation below -- see our methodology for how a recall is confirmed to an outbreak.

Responsible company: MOGO Moringa LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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