FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass I · Food · Recalled July 8, 2026

MOGO PURE MORINGA OLEIFERA CAPSULES recall — MOGO Moringa LLC

Hazard: Product may be contaminated with Salmonella Typhimurium

Class I: most serious — reasonable probability of serious health consequences or death.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
H-1128-2026
Brand
MOGO Moringa
Classification
Class I
Units affected
23,186 bottles
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

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

Affected products

Companies & origin

Recalling firm location
Saint Louis, MO, United States
Firm address
10443 Corbeil Dr, N/A, 63146-5910

Identifying details (verbatim from the notice)

Product codes / lots
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)
Firm notified the public via
E-Mail
FDA event ID
99071
Recall initiated
May 24, 2026
FDA classified
June 29, 2026
FDA report date
July 8, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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