FDAClass IRecall started November 4, 2025

Organic Moringa Leaf Powder Recall: Salmonella

Organic Moringa Leaf Powder (Moringa Powder) , 4 oz. and 1 Kilogram, 4 oz size in a solid plastic container / 1 kg size in a plastic bag in a box. Distributed by: Africa Imports, South Hackensack, NJ 07606

What is the FDA recall status?

The FDA record lists this recall as terminated. This does not establish that a retained recalled product is safe to consume or use. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions.

How FDA enforcement data reports status

Why was Organic Moringa Leaf Powder recalled?

Product tested positive for Salmonella.

What should I do if I have this product?

Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.

Full product description

Organic Moringa Leaf Powder (Moringa Powder) , 4 oz. and 1 Kilogram, 4 oz size in a solid plastic container / 1 kg size in a plastic bag in a box. Distributed by: Africa Imports, South Hackensack, NJ 07606

Which lot codes, UPCs or models are affected?

Lot # SO-71449

Agency record number
H-0222-2026
Product
Organic Moringa Leaf Powder (Moringa Powder) , 4 oz. and 1 Kilogram, 4 oz size in a solid plastic container / 1 kg size in a plastic bag in a box. Distributed by: Africa Imports, South Hackensack, NJ 07606
Recalling firm
Africa Imports
Quantity
31 sold of 1 kg box of Moringa powder- item # M-P697KG from the affected lot
Distribution
The adulterated product was sold to the follwing States: IA, SC, NC, OH, NJ, VA, MS, CA, DC, TX, NY, MI, AZ, MN
Recall started
November 4, 2025
Report date
December 10, 2025
Classification
Class I
Status
Terminated
Agency
FDA (food)
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