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Lower risk Food recall · FDA · Published July 19, 2026

Zen Principle Moringa Leaf Powder Recall: Possible Salmonella Risk

Zen Principle recalls 180-capsule Moringa Leaf Powder due to possible Salmonella contamination. Consumers should check product codes and follow safety steps.

🇺🇸 FDA recall #H-1222-2026FoodZen Principle ›
✎ GovInfoNow plain-language explainer

Zen Principle is recalling its Moringa Leaf Powder dietary supplement because it may contain Salmonella. This poses a risk of foodborne illness, so affected consumers should stop using the product. Read more at govinfonow.com/recall/303182-zen-principle-moringa-leaf-powder-recall-possible-salmonella-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/303182-zen-principle-moringa-leaf-powder-recall-possible-salmonella-risk · Updated August 18, 2026 · Official notice: FDA #H-1222-2026

Cite this page

“Zen Principle Moringa Leaf Powder Recall: Possible Salmonella Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/303182-zen-principle-moringa-leaf-powder-recall-possible-salmonella-risk. Based on FDA recall #H-1222-2026.

The FDA announced on July 19, 2026, that FACTORY6, INC. is recalling Zen Principle Naturals Moringa Leaf Powder dietary supplement due to possible Salmonella contamination. Owners should stop consuming the product immediately.

How to tell if you have it

  • Brand: Zen Principle
  • Product: Zen Principle Naturals Moringa Leaf Powder dietary supplement
  • Form: 900mg capsules, 180 capsules per PET white bottle
  • Pack options: 1-pack (Amazon code/FNSKU X000ZJJ4FT) and 2-pack (twin pack, 360 capsules; Amazon code/FNSKU X00159YJXP)
  • Lot code: A6FF4
  • Best By date: 11/2028
  • Units affected: 2,048 bottles

The hazard

The product may contain Salmonella. The FDA classified the recall as Class I.

Context

GovInfoNow's records show other recent recalls of similar products include Trafa Organic Moringa Leaf Powder Recall: Salmonella Contamination Risk (2026-06-24) and Food to Live Organic Moringa Leaf Powder Recalled Due to Salmonella Contamination (2025-11-11). Additional similar recalls include Total Nutrition Moringa Capsules Recall: Salmonella Contamination Risk (2026-05-22).

How to tell if you have this one

Check for the PET white bottle with 180 capsules (Amazon code X000ZJJ4FT) or 360 capsules (Amazon code X00159YJXP). The lot number is A6FF4 and best by date is November 2028.

  • Brand
    Zen Principle
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the PET white bottle with 180 capsules (Amazon code X000ZJJ4FT) or 360 capsules (Amazon code X00159YJXP).

Where it went and when

Where it was distributed

Distributed in Nevada.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Distributed to Nevada for further distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Nevada.

Recall timeline

FDA published this recall 24 days after the firm started it.

1. Firm started the recall: Jul 19, 202612. FDA classified it Class I: Aug 5, 202623. Published in FDA’s Enforcement Report: Aug 12, 202634. Added to GovInfoNow: Aug 18, 202642026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

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-1222-2026 (July 19, 2026)
  • Plain-language summary written by qwen3:4b on August 18, 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