CLASS I Food recall · Reported 10 Dec 2025 · FDA Enforcement Report

Organic Moringa Leaf Powder (Moringa Powder) recalled by Africa Imports

Africa Imports is recalling Organic Moringa Leaf Powder (Moringa Powder) and 1 Kilogram size in a solid / size in a, distributed in 14 states. The recall was initiated on 4 Nov 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # SO-71449
Quantity recalled31 sold of 1 kg box of Moringa powder- item # M-P697KG from the affected lot

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0222-2026
FDA event ID
97929
Recalling firm
Africa Imports, S Hackensack, NJ
Classification
Class I
Status
Terminated
Recall initiated
4 Nov 2025
FDA classified
2 Dec 2025
Reported
10 Dec 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Herbal Supplements

Timeline

4 Nov 2025Recall initiated by company
2 Dec 2025Classified by FDA+28 days
10 Dec 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product tested positive for Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

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

Where it was distributed

The adulterated product was sold to the follwing States: IA, SC, NC, OH, NJ, VA, MS, CA, DC, TX, NY, MI, AZ, MN

ArizonaCaliforniaDistrict of ColumbiaIowaMichiganMinnesotaMississippiNorth CarolinaNew JerseyNew YorkOhioSouth CarolinaTexasVirginia

Questions about this recall

Why was it recalled?

Product tested positive for Salmonella.

Which lots are affected?

Lot # SO-71449

Where was it sold?

The adulterated product was sold to the follwing States: IA, SC, NC, OH, NJ, VA, MS, CA, DC, TX, NY, MI, AZ, MN

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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