RecallRadar
FDA · FoodClass I

Hemu Trading Inc food recall: Black label with blue lettering. FOOD Korean Food

Listeria

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
98725
Recall initiated
Apr 2, 2026
Classified by FDA
Apr 30, 2026
Posted in Enforcement Report
May 6, 2026
Recalling firm
HEMU TRADING INC
Firm location
Los Angeles, CA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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

product tested positive for Listeria Monocytogenes.

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 2, 2026. FDA classified it 28 days later, on Apr 30, 2026. Distribution reported by FDA: 5 direct account consignees located in CA, FL and MD.

Recalled products (1)

  • H-0686-2026 Class I Ongoing

    Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Product of Korea, Keep Refrigerated. Distributed by Hemu Trading Inc. UPC: 8801234567893

    Codes / lots: Lot code:215

    Quantity: 1056 cases (34 packs/case)

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 98725
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.