RecallRadar
FDA · FoodClass I

Harvest Nyc 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
96724
Recall initiated
Apr 16, 2025
Classified by FDA
May 16, 2025
Posted in Enforcement Report
May 28, 2025
Terminated
Sep 30, 2025
Recalling firm
HARVEST NYC INC
Firm location
Brooklyn, 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 is 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 Apr 16, 2025. FDA classified it 30 days later, on May 16, 2025. Distribution reported by FDA: NY; additional distribution to CT and VT.

Recalled products (1)

  • F-0805-2025 Class I Terminated

    Enoki Mushroom in a 200g, green plastic package marked with UPC Barcode 6975730520101 on the back label and labeled as distributed by Hofood99 Inc., 21903 56th Ave Oakland Gardens, NY 11364

    Codes / lots: No additional coding.

    Quantity: 76 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 96724
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.