Class IOngoingVoluntary: Firm initiated
FACTORY6, INC.: food recall H-1222-2026
FACTORY6, INC. of Lindon, UT recalled Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle.… Reason: Possible Salmonella in Moringa Leaf Powder product. The FDA listed it as Class I in its Enforcement Report dated Aug 12, 2026; distribution: Nevada.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- 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).
- Product quantity
- 2,048 bottles
- Reason for recall
- Possible Salmonella in Moringa Leaf Powder product.
- Codes, lots and dates on the package
- LOT: A6FF4, Best By: 11/2028
- Distribution pattern
- Distributed to Nevada for further distribution.
- Recalling firm
- FACTORY6, INC., Lindon, UT
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Press Release
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jul 19, 2026 |
| Classified by the FDA | Aug 5, 2026 |
| Published in the Enforcement Report | Aug 12, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1222-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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