Enforcement WeeklyRegister of FDA actions · supplements, cosmetics, food
Records as of 2026-09-28 · 202 actions this year · not affiliated with the FDA

Class I · Recall · initiated May 24, 2026 · Ongoing

Other Other

MOGO Moringa capsules sold on Amazon, eBay and Etsy recalled for Salmonella

A St. Louis moringa brand recalled its pure moringa oleifera capsules, sold nationwide through marketplaces and its own site, for possible Salmonella Typhimurium contamination.

The record

Firm
MOGO Moringa LLC, Saint Louis, MO
Product
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 L
Reason, as filed
“Product may be contaminated with Salmonella Typhimurium”
Classification
Class I (Class I: reasonable probability of serious health consequences or death)
Recall number
H-1128-2026
Initiated
May 24, 2026
Posted by FDA
July 8, 2026
Status
Ongoing · Voluntary: Firm initiated
Quantity
23,186 bottles
Distribution
Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)

Verify: search any recall number above in FDA's enforcement report database.

Why it happened, in plain English

The filed reason names a specific serotype, Salmonella Typhimurium, which usually means a laboratory result rather than a precautionary pull. The product is a single-ingredient botanical capsule, so the contamination came in with the powder. Moringa is a dried leaf; drying preserves Salmonella rather than killing it, and capsule filling adds no lethality step.

The distribution line matters for a small brand: nationwide via Amazon, eBay, Etsy and the company site. Marketplace sellers are pulled from listings the day a recall posts, which is often how the brand’s customers find out.

Who else should care

Small botanical brands selling through marketplaces. You are the recalling firm even if a contract manufacturer filled the capsules and a broker sourced the powder, and the marketplace suspension arrives before your customers hear from you.

Check: whether you hold a per-lot microbiological result for the powder in every batch you sold, and whether you can trace each marketplace lot back to it.

Related actions

Written 2026-09-08. Analysis is editorial; the record above is FDA's.