Organic Moringa Leaf Powder (Moringa Powder) , 4 oz. and 1 Kilogram, 4 oz size in a solid plastic container / 1 kg size
Summary
The FDA issued a Class I for Organic Moringa Leaf Powder (Moringa Powder) , 4 oz. and 1 Kilogram, 4 oz size i by Africa Imports. Reason: Product tested positive for Salmonella..
Details
Source
Food Recall
External ID
H-0222-2026
Action Date
2025-12-10
Status
Terminated
Category
food
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
Lot/Code Info: Lot # SO-71449
Quantity Affected: 31 sold of 1 kg box of Moringa powder- item # M-P697KG from the affected lot
Reason for Recall
Product tested positive for Salmonella.
Distribution
The adulterated product was sold to the follwing States: IA, SC, NC, OH, NJ, VA, MS, CA, DC, TX, NY, MI, AZ, MN
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-04
Company
S Hackensack, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Africa Imports) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Africa Imports have FDA actions?
This is the only FDA action we have on record for Africa Imports in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0222-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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