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Lower risk Food recall · FDA · Published January 28, 2026

Why Not Natural Moringa Capsules Recall: Salmonella Contamination Risk

Why Not Natural recalls 120-capsule bottles with lot # A25G051 (expiring 07/2028) due to potential Salmonella contamination. Consumers should check labels and contact the company for details.

🇺🇸 FDA recall #H-0510-2026FoodWhy Not Natural ›
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Contact the company

Recalling firmArt Monkey LLC dba Why Not Natural4315 Alba Rd · Houston, TX 77018-4407
✎ GovInfoNow plain-language explainer

Why Not Natural is recalling 120-capsule bottles of Moringa capsules with lot number A25G051 that may be contaminated with Salmonella. This poses a risk of foodborne illness if consumed. Read more at govinfonow.com/recall/6767-why-not-natural-moringa-capsules-recall-salmonella-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/6767-why-not-natural-moringa-capsules-recall-salmonella-contamination-risk · Updated August 17, 2026 · Official notice: FDA #H-0510-2026

Cite this page

“Why Not Natural Moringa Capsules Recall: Salmonella Contamination Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6767-why-not-natural-moringa-capsules-recall-salmonella-contamination-risk. Based on FDA recall #H-0510-2026.

The FDA announced on Jan. 28, 2026, that Art Monkey LLC dba Why Not Natural is recalling Why Not Natural Moringa Capsules due to potential Salmonella contamination. The firm initiated the voluntary Class I recall affecting 8,500 bottles distributed nationwide.

How to tell if you have it

  • Brand: Why Not Natural
  • Product: Why Not Natural Moringa Capsules 120 capsule bottle
  • Lot code: A25G051
  • Expiration date: 07/2028

The hazard

The product poses a potential to be contaminated with Salmonella, according to the FDA. The recall classification is Class I.

Context

GovInfoNow's records show Art Monkey LLC dba Why Not Natural has issued other recent recalls of similar products including Total Nutrition Moringa Capsules Recall: Salmonella Contamination Risk (2026-05-22), MOGO Moringa Capsules Recall: Salmonella Contamination Risk (2026-05-24), and Rosabella Moringa Capsules Recall: Salmonella Contamination Risk (2026-02-13).

How to tell if you have this one

Check for a 120-capsule bottle labeled with lot number A25G051 and expiration date 07/2028 on the bottom. The product was sold from the manufacturer's date of production.

  • Brand
    Why Not Natural
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for lot number A25G051 and expiration date 07/2028 on the bottom of the bottle.

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: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Jan 28, 202612. FDA classified it Class I: Feb 13, 202623. Published in FDA’s Enforcement Report: Feb 25, 202634. FDA terminated the recall: Apr 3, 202642026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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-0510-2026 (January 28, 2026)
  • Plain-language summary written by qwen3:4b on August 17, 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