Enoki Mushroom in a 200g, green and clear plastic package marked with UPC Barcode 6 976532 310051 on the back label; a p
Summary
The FDA issued a Class I for Enoki Mushroom in a 200g, green and clear plastic package marked with UPC Barcod by HOFOOD99 INC.. Reason: Product may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
H-0261-2025
Action Date
2025-07-23
Status
Terminated
Category
food
Product Description
Enoki Mushroom in a 200g, green and clear plastic package marked with UPC Barcode 6 976532 310051 on the back label; a picture of enoki mushrooms is outlined in green on the front of the package
Lot/Code Info: No additional coding.
Quantity Affected: 90 boxes
Reason for Recall
Product may be contaminated with Listeria monocytogenes.
Distribution
CA (with additional downstream distribution)
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-10
Company
Bayside Hills, NY
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 98 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 (HOFOOD99 INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does HOFOOD99 INC. have FDA actions?
This is the only FDA action we have on record for HOFOOD99 INC. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0261-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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