Stop using nowFood recall · FDA · Published November 4, 2025
Africa Imports Moringa Powder Recall: Salmonella Risk
Africa Imports recalls 4 oz and 1 kg organic moringa leaf powder due to Salmonella contamination. Consumers should stop using affected products immediately.
“Africa Imports Moringa Powder Recall: Salmonella Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/7005-africa-imports-moringa-powder-recall-salmonella-risk. Based on FDA recall #H-0222-2026.
Africa Imports recalled Organic Moringa Leaf Powder distributed by the company because it tested positive for Salmonella, according to the FDA. The Food and Drug Administration announced the recall on Nov. 4, 2025.
The product tested positive for Salmonella. The FDA classified the recall as Class I.
Context
GovInfoNow's records show other recent recalls of similar products include Trafa Organic Moringa Leaf Powder Recall (2026-06-24), Bulk & Organic Moringa Powder Recall (2025-10-31), and Food to Live Organic Moringa Leaf Powder Recalled (2025-11-11).
How to tell if you have this one
Check for the 4 oz size in a solid plastic container or 1 kg size in a plastic bag. Products were distributed by Africa Imports with lot number SO-71449.
Brand
Africa Imports
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using Product
Immediately stop using the recalled organic moringa leaf powder products that tested positive for Salmonella.
Where it went and when
Where it was distributed
Distributed in 13 states and D.C..
Listed by the agency
Not listed
FDA distribution: “The adulterated product was sold to the follwing States: IA, SC, NC, OH, NJ, VA, MS, CA, DC, TX, NY, MI, AZ, MN” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, District of Columbia, Iowa, Michigan, Minnesota, Mississippi, New Jersey, New York, North Carolina, Ohio, South Carolina, Texas, Virginia.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0222-2026 (November 4, 2025)
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.