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Lower risk Food recall · FDA · Published May 24, 2026

MOGO Moringa Capsules Recall: Salmonella Contamination Risk

MOGO recalls 180-count Moringa capsules due to potential Salmonella Typhimurium contamination. Consumers should stop using affected lots to avoid foodborne illness.

🇺🇸 FDA recall #H-1128-2026FoodMOGO ›
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Recalling firmMOGO Moringa LLC10443 Corbeil Dr · Saint Louis, MO 63146-5910
✎ GovInfoNow plain-language explainer

MOGO is recalling 180-count Moringa capsules that may contain Salmonella Typhimurium. This contamination could cause foodborne illness if consumed. Affected products have specific lot codes and expiration dates. Read more at govinfonow.com/recall/6202-mogo-moringa-capsules-recall-salmonella-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/6202-mogo-moringa-capsules-recall-salmonella-contamination-risk · Updated August 9, 2026 · Official notice: FDA #H-1128-2026

Cite this page

“MOGO Moringa Capsules Recall: Salmonella Contamination Risk.” GovInfoNow, updated August 9, 2026. https://govinfonow.com/recall/6202-mogo-moringa-capsules-recall-salmonella-contamination-risk. Based on FDA recall #H-1128-2026.

MOGO Moringa LLC voluntarily recalled MOGO PURE MORINGA OLEIFERA CAPSULES due to potential Salmonella Typhimurium contamination, the FDA said on May 24, 2026. The Class I recall affects 23,186 bottles sold nationwide via ecommerce platforms.

How to tell if you have it

  • Brand: MOGO
  • Product: MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE
  • Lot codes: 15525AA (exp date: 6/2027), 00926AA (exp date: 1/2028)
  • Sold via Amazon, Ebay, Etsy, and mogomiranga.com

The hazard

The product may be contaminated with Salmonella Typhimurium. The FDA classified the recall as Class I.

Context

GovInfoNow's records show other recent recalls of similar products include Total Nutrition Moringa Capsules Recall (2026-05-22), Rosabella Moringa Capsules Recall (2026-02-13), and Why Not Natural Moringa Capsules Recall (2026-01-28).

How to tell if you have this one

Check the lot code on the capsule packaging: 15525AA (expires 6/2027) or 00926AA (expires 1/2028). The product is sold as a dietary supplement with 180 capsules.

  • Brand
    MOGO
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Code

    Look for lot codes 15525AA (expires 6/2027) or 00926AA (expires 1/2028) on the capsule packaging.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com)” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 45 days after the firm started it.

1. Firm started the recall: May 24, 202612. FDA classified it Class I: Jun 29, 202623. Published in FDA’s Enforcement Report: Jul 8, 202632026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-1128-2026 (May 24, 2026)
  • Plain-language summary written by qwen3:4b on August 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA