RecallHawk
Class I Recall

Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 2 lb.,

Lexunder Inc

Summary

The FDA issued a Class I for Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable by Lexunder Inc. Reason: Contaminated with Salmonella.

Details

Source

Food Recall

External ID

H-0309-2026

Action Date

2025-12-24

Status

Terminated

Category

food

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

Lot/Code Info: lot codes starting with SO-69006 and ending with SO-72558

Quantity Affected: 701 units total

Reason for Recall

Contaminated with Salmonella

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

Type: Voluntary: Firm initiated

Recall Initiated: 2025-11-11

Company

Lexunder Inc

Brooklyn, NY

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 87 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Lexunder Inc has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lexunder Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lexunder Inc have FDA actions?

Lexunder Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0309-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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