FDA Recall United States Terminated Historical recordClass I
Lexunder Inc
- Product
- Food to Live brand ORGANIC SUPERGREENS POWDER MIX, packaged…
- Published
- December 24, 2025
- Distribution
- Multiple states
Lexunder Inc Recall: Contaminated with Salmonella
United States
TerminatedClass I
- Company
- Lexunder Inc
- Product
- Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged hea…
- Recall date
- November 11, 2025
- Terminated
- March 11, 2026
- Source
- FDA
Reason for recall
Contaminated with Salmonella
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 2 lb., 4 lb., 8 lb., 16 lb., and 44 lb. bags; Ingredients: ORGANIC MORINGA LEAF POWDER; UPC: 8 oz - 840374833268 1 lb. - 840374812881 2 lb. - 840374813109 4 lb. - 840374810283 8 lb. - 840374833275 12 lb. - 840374812898 16 lb. - 840374812904 44 lb. - 840374833282 | Not published in this source record | 701 units total | lot codes starting with SO-69006 and ending with SO-72558 |
Distribution
- AK
- AL
- AR
- AZ
- CA
- CO
- CT
- DE
- FL
- GA
- GU
- HI
- ID
- IL
- IN
- KS
- MA
- MD
- ME
- MI
- MN
- MO
- MT
- NC
- NJ
- NM
- NV
- NY
- OH
- OR
- PA
- SC
- TN
- TX
- UT
- VA
- WA
- WI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0309-2026
- Event ID
- 97966
- Status
- Terminated
- Classification
- Class I
- Company
- Lexunder Inc
- Product description
- Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 2 lb., 4 lb., 8 lb., 16 lb., and 44 lb. bags; Ingredients: ORGANIC MORINGA LEAF POWDER; UPC: 8 oz - 840374833268 1 lb. - 840374812881 2 lb. - 840374813109 4 lb. - 840374810283 8 lb. - 840374833275 12 lb. - 840374812898 16 lb. - 840374812904 44 lb. - 840374833282
- Quantity
- 701 units total
- Reason
- Contaminated with Salmonella
- Recall initiation date
- November 11, 2025
- Report date
- December 24, 2025
- Classification date
- Not published in this source record
- Termination date
- March 11, 2026
- Distribution pattern
- AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, ID, IL, IN, KS, MA, MD, ME, MI, MN, MO, MT, NC, NJ, NM, NV, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI
- UPC, lot, and code information
- lot codes starting with SO-69006 and ending with SO-72558
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 97966 with 1 other product entry in Public Health Trace.
Responsible company: Lexunder Inc
Other recalls from Lexunder Inc
FDA Recall United States Terminated Historical recordClass I
Lexunder Inc
- Product
- Food to Live brand ORGANIC SUPERGREENS POWDER MIX, packaged…
- Published
- December 24, 2025
- Distribution
- Multiple states
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alaska | 1 |
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Delaware | 1 |
| Florida | 1 |
| Georgia | 1 |
| Guam | 1 |
| Hawaii | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Montana | 1 |
| North Carolina | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
