Class ITerminatedVoluntary: Firm initiated
Africa Imports: food recall H-0222-2026
Africa Imports of S Hackensack, NJ recalled Organic Moringa Leaf Powder (Moringa Powder) , 4 oz. and 1 Kilogram, 4 oz size in a solid plastic container / 1 kg… Reason: Product tested positive for Salmonella. The FDA listed it as Class I in its Enforcement Report dated Dec 10, 2025; distribution: Arizona, California, District of Columbia, Iowa, Michigan, Minnesota, Mississippi, North Carolina, New Jersey, New York, Ohio, South Carolina, Texas, Virginia.
Record status as published: Terminated (terminated Jan 9, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- 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
- Product quantity
- 31 sold of 1 kg box of Moringa powder- item # M-P697KG from the affected lot
- Reason for recall
- Product tested positive for Salmonella.
- Codes, lots and dates on the package
- Lot # SO-71449
- Distribution pattern
- The adulterated product was sold to the follwing States: IA, SC, NC, OH, NJ, VA, MS, CA, DC, TX, NY, MI, AZ, MN
- Recalling firm
- Africa Imports, S Hackensack, NJ
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Nov 4, 2025 |
| Classified by the FDA | Dec 2, 2025 |
| Published in the Enforcement Report | Dec 10, 2025 |
| Terminated | Jan 9, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0222-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.