CLASS I Food recall · Reported 6 Nov 2024 · FDA Enforcement Report

(Principal Display) Enoki Mushroom Champignons d'enoki recalled

Enoki King Mushroom Farm is recalling (Principal Display) Enoki Mushroom Champignons d'enoki, distributed in 7 states. The recall was initiated on 10 Oct 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes4877
Quantity recalled864 cases

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-0075-2025
FDA event ID
95522
Recalling firm
Enoki King Mushroom Farm, Ventura, CA
Classification
Class I
Status
Terminated
Recall initiated
10 Oct 2024
FDA classified
29 Oct 2024
Reported
6 Nov 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Listeria
Product category
Mushrooms

Timeline

10 Oct 2024Recall initiated by company
29 Oct 2024Classified by FDA+19 days
6 Nov 2024Published in enforcement report+8 days

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

Reason for recall

The product was found to have 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

(Principal Display) ENOKI MUSHROOM Champignons d'enoki Net Wt: 150g (5.3oz) in a clear plastic packaged. (Back Display) UPC 860011505600 Keep Refrigerated Garder Au Froid Distributed by: Global Fresh Marketing Commerce, CA 90040

Where it was distributed

CA, MD, NY, NJ, VA, MA, and NC

CaliforniaMassachusettsMarylandNorth CarolinaNew JerseyNew YorkVirginia

Questions about this recall

Is (Principal Display) Enoki Mushroom Champignons d'enoki recalled?

Yes. Enoki King Mushroom Farm recalled (Principal Display) Enoki Mushroom Champignons d'enoki on 10 Oct 2024. The recall is Class I and its status is Terminated. Recall number F-0075-2025.

Why was it recalled?

The product was found to have Listeria monocytogenes

Which lots are affected?

4877

Where was it sold?

CA, MD, NY, NJ, VA, MA, and NC

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 21 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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