RecallHawk
Class I Recall

Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intend

FACTORY6, INC.

Summary

The FDA issued a Class I for Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 1 by FACTORY6, INC.. Reason: Possible Salmonella in Moringa Leaf Powder product..

Details

Source

Food Recall

External ID

H-1222-2026

Action Date

2026-08-12

Status

Ongoing

Category

food

Product Description

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).

Lot/Code Info: LOT: A6FF4, Best By: 11/2028

Quantity Affected: 2,048 bottles

Reason for Recall

Possible Salmonella in Moringa Leaf Powder product.

Distribution

Distributed to Nevada for further distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-07-19

Company

FACTORY6, INC.

Lindon, UT

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 36 food recalls issued in the same week, part of 73 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (FACTORY6, INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does FACTORY6, INC. have FDA actions?

This is the only FDA action we have on record for FACTORY6, INC. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1222-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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