Fresh Recalls

FDAClass I · Food · Recall H-1222-2026 · Recalled August 12, 2026

Zen Principle Naturals Moringa Leaf Powder dietary supplement recall — FACTORY6, INC.

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Zen Principle Naturals Moringa Leaf Powder dietary supplement
Company / brand
FACTORY6
Lot / serial / date codes
LOT: A6FF4, Best By: 11/2028
Distribution
Distributed to Nevada for further distribution.
Agency product description and boundaries

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).

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Possible Salmonella in Moringa Leaf Powder product.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Zen Principle Naturals Moringa Leaf Powder dietary supplement

3. Open the official notice or contact

Official recall ID
H-1222-2026
Brand
FACTORY6
Classification
Class I
Units affected
2,048 bottles
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Lindon, UT, United States
Firm address
632 N 2000 W Ste 100, 84042-1798

Identifying details (verbatim from the notice)

Product codes / lots
LOT: A6FF4, Best By: 11/2028
Distribution
Distributed to Nevada for further distribution.
Firm notified the public via
Press Release
FDA event ID
99425
Recall initiated
July 19, 2026
FDA classified
August 5, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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