FACTORY6, Inc. food recall: Zen Principle Naturals Moringa Leaf Powder dietary supplement
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 99425
- Recall initiated
- Jul 19, 2026
- Classified by FDA
- Aug 5, 2026
- Posted in Enforcement Report
- Aug 12, 2026
- Recalling firm
- FACTORY6, INC.
- Firm location
- Lindon, UT, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Press Release
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Possible Salmonella in Moringa Leaf Powder product.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Jul 19, 2026. FDA classified it 17 days later, on Aug 5, 2026. Distribution reported by FDA: Distributed to Nevada for further distribution.
Recalled products (1)
H-1222-2026 Class I Ongoing
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).
Codes / lots: LOT: A6FF4, Best By: 11/2028
Quantity: 2,048 bottles
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 99425
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.