Recall archive / FDA food enforcement
Foods Alive organic moringa leaf powder, 8oz pouch, UPC 8 91551 00092 8 — FDA record H-1336-2026
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 26, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Foods Alive organic moringa leaf powder, 8oz pouch, UPC 8 91551 00092 8
- Reason
- Potential Salmonella contamination
- Classification
- Class I
- Recalling firm
- FOODS ALIVE INC.
- Quantity
- 1691 pouches
- Agency-reported status
- Ongoing
- Source record identifier
- H-1336-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Freshest by 110127 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Nationwide US and UAE. The recalled organic moringa leaf powder was distributed nationwide in retail stores and through online sellers including but not limited to www.foodsalive.com.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Sep 23, 2026
- Recall initiation date
- Aug 26, 2026
- Center classification date
- Sep 11, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.