RecallRadar
FDA · FoodClass I

Nassar Investment Company LLC food recall: Malazi 100% PURE SUDANESE SESAME Tahina G.W.: 1K.g

Salmonella

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
98923
Recall initiated
Apr 30, 2026
Classified by FDA
May 29, 2026
Posted in Enforcement Report
Jun 10, 2026
Recalling firm
Nassar Investment Company LLC
Firm location
Morrisville, NC, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Telephone
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.

View the official FDA record ↗

Reason for recall

Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test 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 Apr 30, 2026. FDA classified it 29 days later, on May 29, 2026. Distribution reported by FDA: Product was shipped to MI & NC.

Recalled products (1)

  • H-0860-2026 Class I Ongoing

    Malazi 100% PURE SUDANESE SESAME Tahina G.W.: 1K.g UPC 6 224011 088244 Produced by: AL-MALAZ COMPANY FOR TRADE AND INDUSTRY Piece No. 110-250 acres area Badr City - Egypt

    Codes / lots: PROD: 31/12/2024 EXP: 30/12/2026

    Quantity: 11cs/6/ 2lb bottles

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 98923
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.