Zen Principle Naturals Moringa Leaf Powder Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
FACTORY6, INC. is recalling 2,048 bottles of Zen Principle Naturals Moringa Leaf Powder due to possible Salmonella contamination.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 18, 2026 and geographically references Nevada. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
What Happened
FACTORY6, INC. has initiated a voluntary recall of Zen Principle Naturals Moringa Leaf Powder dietary supplement due to possible Salmonella in the Moringa Leaf Powder product. The recall is classified as Class I by the FDA.
Which Products Are Affected
The affected product is Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. It is offered as a 1-pack (180 capsules; Amazon code/FNSKU X000ZJJ4FT) and as a 2-pack (360 capsules; Amazon code/FNSKU X00159YJXP). The product was manufactured for Zen Principle, 774 Mays Blvd, Incline Village, NV 89451. Affected units are from LOT: A6FF4, Best By: 11/2028. A total of 2,048 bottles were distributed to Nevada for further distribution.
What You Should Do
Consumers should verify the lot number on purchased bottles. The recalling firm initiated the recall via press release.
Why This Matters
This is an ongoing Class I recall involving a food product distributed in Nevada.
Source
FDA recall number H-1222-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,052 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 18, 2026.
Frequently Asked Questions
Common questions about this FDA recall.