RecallRadar
FDA · FoodClass I

HOFOOD99 Inc. food recall: Enoki Mushroom in a 200g

ListeriaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
97054
Recall initiated
Jun 10, 2025
Classified by FDA
Jul 11, 2025
Posted in Enforcement Report
Jul 23, 2025
Terminated
Sep 30, 2025
Recalling firm
HOFOOD99 INC.
Firm location
Bayside Hills, NY, 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 may be contaminated with 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 Jun 10, 2025. FDA classified it 31 days later, on Jul 11, 2025. Distribution reported by FDA: CA (with additional downstream distribution)

Recalled products (1)

  • H-0261-2025 Class I Terminated

    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

    Codes / lots: No additional coding.

    Quantity: 90 boxes

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 97054
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.