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Ongoing FDAEvent 99425 (2 months ago)

Zen Principle Naturals Moringa Leaf Powder Dietary Supplement

Zen Principle Naturals Moringa Leaf Powder dietary supplement may be contaminated with Salmonella, which can cause serious infections.

High risk

There is a reasonable chance that eating it could cause serious health problems or death.

FDA Class I recall · How risk is rated

2 photos

What to do

What happened

FACTORY6, INC. of Lindon, Utah announced on July 19, 2026, a voluntary recall of Zen Principle Naturals Moringa Leaf Powder dietary supplement, sold as 900mg capsules in PET white bottles of 180 capsules, because the product has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections. The recall covers 2,048 bottles distributed to Nevada for further distribution.

The product was manufactured for Zen Principle at 774 Mays Blvd, Incline Village, NV 89451, and is offered as a 1-pack (180 capsules) and a 2-pack (360 capsules). The FDA added the recall to its Enforcement Report on August 5, 2026, and it was in the weekly enforcement report on August 12, 2026.

Summary by Recall Canary from the FDA notice.

What to do

If a code on your package matches:

  1. Consumers who purchased Zen Principle® Moringa Capsules, Lot A6FF4, are urged to stop using the product.
  2. Dispose of it.
  3. To request a refund or ask any questions, consumers may contact the company at 775-451-6171 from 9 AM to 5 PM Pacific Time, or by email at info@zenprinciple.com.

Is yours affected?

Match the lot code and best-by date listed under your product.

  1. Zen Principle® brand Moringa Capsules

    Lot code
    • A6FF4
    Best-by
    11/2028

Label photos, 2

Details

Company began the recall
Sold in

Distributed to Nevada for further distribution.

Event ID
99425
Recall No.
H-1222-2026
Company
FACTORY6, INC.Lindon, Utah
Quantity recalled
2,048 bottles
Recall type
Voluntary: Firm initiated
Customers told by
Press Release
  1. Company began the recall · Announced by the company

  2. Listed on Recall Canary

  3. Added to FDA's Enforcement Report · Classified by FDA

  4. In FDA's weekly enforcement report

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 7, 2026 · primary source: U.S. Food and Drug Administration