The Recall Desk
Agency classClass IOur severity:SevereFDA (Food)·H-1222-2026·Announced 2026-08-12

Moringa Leaf Powder Dietary Supplement Recalled Due to Potential Salmonella Contamination

Zen Principle Naturals Moringa Leaf Powder is being recalled because it may contain Salmonella. This affects specific lots of 900mg capsules.

The agency’s classification

FDA (Food): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classified this recall as Class I — a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. On that classification alone this is scored Severe; a score of Critical is reserved for recalls where a death or serious injury was reported. The agency gives the reason as: "Possible Salmonella in Moringa Leaf Powder product."

Plain-English summary

Zen Principle Naturals Moringa Leaf Powder dietary supplement (900mg capsules) is being recalled due to the potential presence of Salmonella.

This recall affects 180-capsule PET white bottles with Lot A6FF4 and a Best By date of 11/2028. The affected products include single 1-packs and twin 2-packs distributed in Nevada.

Consumers should stop using the affected product and contact the manufacturer or retailer for further information.

The recalled product

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…
Manufacturer
FACTORY6, INC.
Affected units
2,048

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • LOT: A6FF4
  • Best By: 11/2028

Distribution

Distributed in 1 state:

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