Forest Mushroom Food Inc. Recall: Michigan Department of Agriculture and Rural Development sampled Enoki mushrooms and found some samples to be positive for Listeria monocytogenes. - F-0476-2021

🇺🇸 United States

1. April 20, 2021 - Recall initiated
2. May 12, 2021 - Reported by source
3. February 18, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0476-2021

Event ID

87761

Status

Terminated

Classification

Class I

Company

Forest Mushroom Food Inc.

Product description

Guan's Enoki Mushroom - Champigons d'enoki; Net Wt./ Poids Net 200 g/ 7.05 oz.; 25 individual packages per box. Distributed by Guan's Mushroom Co., Los Angeles, Ca 90040 Ingredients - 100% Fresh Enoki Mushroom - Keep Refrigerated. Product of China UPC 8 10023 17030 3

Quantity

RY3428A  3519 boxes RY3434A  3419 boxes

Reason

Michigan Department of Agriculture and Rural Development sampled Enoki mushrooms and found some samples to be positive for Listeria monocytogenes.

Recall initiation date

April 20, 2021

Report date

May 12, 2021

Classification date

Not published in this source record

Termination date

February 18, 2022

Distribution pattern

Nationwide

UPC, lot, and code information

Product Code RY3428A, Lot Number 1753601 Product Code RY3434A, Lot Number 1783001 Product number 00088

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Forest Mushroom Food Inc.

Other recalls from Forest Mushroom Food Inc.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of February 18, 2022.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

• Email
• X / Twitter
• Facebook