Food recall

HEMU TRADING INC recall: Black label with blue lettering

HEMU TRADING INC, of Los Angeles, CA, recalled Black label with blue lettering. The FDA's reason: “product tested positive for Listeria Monocytogenes.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on April 2, 2026, and the FDA first listed it in its Enforcement Report of May 6, 2026. The recall is still going on.

How serious

Class I

It could cause serious harm or death

Why

Listeria

Status

Ongoing

The recall

Company
HEMU TRADING INC (Los Angeles, CA)
Reason, in FDA's words
“product tested positive for Listeria Monocytogenes.”
Where it was sold
5 direct account consignees located in CA, FL and MD.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
98725

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0686-2026 Class I

    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: Lot code:215

    Quantity: 1056 cases (34 packs/case)

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of May 6, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.