Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM

HEMU TRADING INC has recalled Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on May 6, 2026 and was initiated on April 2, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, with approximately 1056 cases (34 packs/case) affected. The company behind the recall is HEMU TRADING INC, based in Los Angeles, CA. The FDA describes the product as: “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”

Why was Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM recalled?

According to the FDA, the stated reason for the recall is: “product tested positive for Listeria Monocytogenes.” In plain terms, this recall relates to Listeria.

Listeria monocytogenes is a bacterium that can grow even at refrigerator temperatures, which makes it a particular concern in ready-to-eat foods. Health authorities warn that it can cause a serious infection called listeriosis, and that pregnant people, newborns, older adults, and those with weakened immune systems are especially vulnerable. This is why products potentially contaminated with Listeria are often recalled quickly.

What should you do?

If you think you may have bought Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, compare it against the product description and identifying codes (Lot code:215) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact HEMU TRADING INC or your local health authority.

About this recall

This recall was distributed in CA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.