Africa Imports food recall: Organic Moringa Leaf Powder
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97929
- Recall initiated
- Nov 4, 2025
- Classified by FDA
- Dec 2, 2025
- Posted in Enforcement Report
- Dec 10, 2025
- Terminated
- Jan 9, 2026
- Recalling firm
- Africa Imports
- Firm location
- S Hackensack, NJ, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Product tested positive for Salmonella.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Nov 4, 2025. FDA classified it 28 days later, on Dec 2, 2025. Distribution reported by FDA: The adulterated product was sold to the follwing States: IA, SC, NC, OH, NJ, VA, MS, CA, DC, TX, NY, MI, AZ, MN
Recalled products (1)
H-0222-2026 Class I Terminated
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
Codes / lots: Lot # SO-71449
Quantity: 31 sold of 1 kg box of Moringa powder- item # M-P697KG from the affected lot
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 97929
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.