CLASS I Food recall · Reported 16 Jun 2021 · FDA Enforcement Report

Enoki Mushroom with orange bottom recalled by Rainfield Marketing Group

Rainfield Marketing Group is recalling Enoki Mushroom with orange bottom, distributed in California, Maryland, Texas. The recall was initiated on 28 May 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNo codes
Quantity recalled1200 ctn

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0748-2021
FDA event ID
88015
Recalling firm
Rainfield Marketing Group, Vernon, CA
Brand
Enoki
Classification
Class I
Status
Terminated
Recall initiated
28 May 2021
FDA classified
28 Jun 2021
Reported
16 Jun 2021
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Mushrooms

Timeline

28 May 2021Recall initiated by company
16 Jun 2021Published in enforcement report+19 days
28 Jun 2021Classified by FDA+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

California Department of Public Health sampled Enoki mushrooms at retail with a positive result for Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Enoki Mushroom, 150g clear plastic bag with orange bottom; UPC 085412004020 Product of Korea Do no consume Raw Distributed by Rainfield Marketing Group

Where it was distributed

U.S. distribution to the following: CA, TX, MD No foreign distribution.

CaliforniaMarylandTexas

Questions about this recall

Why was it recalled?

California Department of Public Health sampled Enoki mushrooms at retail with a positive result for Listeria monocytogenes.

Which lots are affected?

No codes

Where was it sold?

U.S. distribution to the following: CA, TX, MD No foreign distribution.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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