Product Wiki · Recalls · U.S. FDA — Food Enforcement

Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg… — recall H-1222-2026

U.S. FDA — Food Enforcement · United States · 2026-07-19 · Class I

As described by U.S. FDA — Food Enforcement: 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 cap

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked on this page. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Food Enforcement
Recall identifier
H-1222-2026
Date of alert
2026-07-19
Country / jurisdiction
United States
Risk level
Class I
Notice type
recall
Brand
FACTORY6, INC.
Product category
food
Product type
Food
Recall status
Ongoing — the recall is still in progress
Initiated by
Voluntary: Firm initiated
Distribution
Distributed to Nevada for further distribution.
🔴 Serious hazard — Reported risk: Possible Salmonella in Moringa Leaf Powder product.
What to do

Check whether your product matches this notice (name, batch, dates). If it does, stop using it and follow the instructions in the official notice — refund, return, repair or disposal are set by the issuing authority and the business, and they differ per recall. Official notice from U.S. FDA — Food Enforcement →

Primary source: https://api.fda.gov/food/enforcement.json?search=recall_number:%22H-1222-2026%22

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.