CLASS I ONGOING Food recall · Reported 12 Aug 2026 · FDA Enforcement Report
Zen Principle Naturals Moringa Leaf Powder dietary recalled by Factory6
Factory6 is recalling Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules per PET, distributed in Nevada. The recall was initiated on 19 Jul 2026 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-1222-2026
- FDA event ID
- 99425
- Recalling firm
- Factory6, Lindon, UT
- Brand
- Zen Principle
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 19 Jul 2026
- FDA classified
- 5 Aug 2026
- Reported
- 12 Aug 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Salmonella
- Product category
- Herbal Supplements
Timeline
| 19 Jul 2026 | Recall initiated by company | |
| 5 Aug 2026 | Classified by FDA | +17 days |
| 12 Aug 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Possible Salmonella in Moringa Leaf Powder product.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
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).
Where it was distributed
Distributed to Nevada for further distribution.
Stores named: Amazon, Online Retailers
Questions about this recall
Why was it recalled?
Possible Salmonella in Moringa Leaf Powder product.
Which lots are affected?
LOT: A6FF4, Best By: 11/2028
Where was it sold?
Distributed to Nevada for further distribution.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other Herbal Supplements recalls
All 509| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Lacnola; Small recalled by The Hampton Grocer | The Hampton Grocer | Salmonella | Nationwide |
| Food | ANNOUNCED | Moringa Leaf Powder recalled by Foods AliveFoods Alive | Foods Alive | Salmonella | Nationwide |
| Food | CLASS II | A-L Complex Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS II | A-P Herbal Supplement May Contain Nuts recalled by Byron White FormulasByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS II | A-fng Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |