---
title: "Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules... — FDA record H-1222-2026 | Is It on Recall"
description: "Possible Salmonella in Moringa Leaf Powder product."
url: https://isitonrecall.com/recall/fda-food-h-1222-2026-zen-principle-naturals-moringa-leaf-powder-dietary-supplement-900mg-capsules-180-capsules-per-pet-wh/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Int... — FDA record H-1222-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 19, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per day. Route of Administration: OraI. Manufactured for Zen Principle 774 Mays Blvd Incline Village, NV 89451. The product is offered as a 1-pack (180 capsules; Amazon code/FNSKU X000ZJJ4FT) and as a 2-pack (twin pack, 360 capsules; Amazon code/FNSKU X00159YJXP).
- **Reason**: Possible Salmonella in Moringa Leaf Powder product.
- **Classification**: Class I
- **Recalling firm**: FACTORY6, INC.
- **Quantity**: 2,048 bottles
- **Agency-reported status**: Ongoing
- **Source record identifier**: H-1222-2026

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1222-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | LOT: A6FF4, Best By: 11/2028 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Distributed to Nevada for further distribution.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Nevada](https://isitonrecall.com/state/nevada/)

## Dates in the source

- **Report date**: Aug 12, 2026
- **Recall initiation date**: Jul 19, 2026
- **Center classification date**: Aug 5, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1222-2026%22)

## Related records

[Supplements records](https://isitonrecall.com/product/supplements/) [Supplements records](https://isitonrecall.com/category/supplements/) [FACTORY6, INC. records](https://isitonrecall.com/brand/factory6-inc/)