Not medical advice · Not affiliated with FDA
Supplement Recall Tracker

All recall records

H-1222-2026

FACTORY6, INC.

Data retrieved 2026-10-27T22:06:49.008Z

Site-assigned category (for this product recall): Contamination

Independent website; not affiliated with or endorsed by FDA. Recall information is attributed to the linked FDA record. Categories are assigned by this website using keyword rules; they are not FDA classifications or independent legal findings and may be incomplete or incorrect. A category summarizes the stated reason for the identified product recall, not a finding about the firm generally or its other products. FDA’s original reason text appears below.

Official openFDA record · FDA recalls and safety alerts

Fields as reported by FDA

Dates are formatted YYYY-MM-DD. “Not reported” means the field was absent or empty.

recall_number
H-1222-2026
event_id
99425
recalling_firm
FACTORY6, INC.
city
Lindon
state
UT
country
United States
product_description
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).
reason_for_recall
Possible Salmonella in Moringa Leaf Powder product.
classification
Class I
FDA-reported status (not current status)
Ongoing
FDA does not update this status after recall classification. It may not reflect whether the recall is currently ongoing, completed, or terminated.
voluntary_mandated
Voluntary: Firm initiated
distribution_pattern
Distributed to Nevada for further distribution.
product_quantity
2,048 bottles
code_info
LOT: A6FF4, Best By: 11/2028
recall_initiation_date
2026-07-19
report_date
2026-08-12
termination_date
Not reported