Zen Principle Naturals Moringa Leaf Powder dietary supplement Recall: Salmonella
Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per…
What is the FDA recall status?
The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.
Why was Zen Principle Naturals Moringa dietary supplement recalled?
Possible Salmonella in Moringa Leaf Powder product.
What should I do if I have this product?
Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.
Full 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).
Which lot codes, UPCs or models are affected?
LOT: A6FF4, Best By: 11/2028
- Agency record number
- H-1222-2026
- Product
- Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per…
- Recalling firm
- FACTORY6, INC.
- Quantity
- 2,048 bottles
- Distribution
- Distributed to Nevada for further distribution.
- Recall started
- July 19, 2026
- Report date
- August 12, 2026
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (food)