Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Product of Korea, Keep Re
Summary
The FDA issued a Class I for Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear pl by HEMU TRADING INC. Reason: product tested positive for Listeria Monocytogenes..
Details
Source
Food Recall
External ID
H-0686-2026
Action Date
2026-05-06
Status
Ongoing
Category
food
Product Description
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
Lot/Code Info: Lot code:215
Quantity Affected: 1056 cases (34 packs/case)
Reason for Recall
product tested positive for Listeria Monocytogenes.
Distribution
5 direct account consignees located in CA, FL and MD.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-02
Company
Los Angeles, CA
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 19 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (HEMU TRADING INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does HEMU TRADING INC have FDA actions?
This is the only FDA action we have on record for HEMU TRADING INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0686-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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