Organic Moringa Leaf Powder recall
Recalled by Africa Imports · S Hackensack, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product tested positive for Salmonella.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
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
Quantity: 31 sold of 1 kg box of Moringa powder- item # M-P697KG from the affected lot
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot # SO-71449
Where it was sold
Arizona California District of Columbia Iowa Michigan Minnesota Mississippi North Carolina New Jersey New York Ohio South Carolina Texas Virginia
FDA's distribution note: The adulterated product was sold to the follwing States: IA, SC, NC, OH, NJ, VA, MS, CA, DC, TX, NY, MI, AZ, MN
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Africa Imports
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 4, 2025
- In FDA report of
- Dec 10, 2025
- Terminated
- Jan 9, 2026
- FDA recall number
- H-0222-2026 · event 97929
- Official record
- FDA enforcement report search