CLASS I Food recall · Reported 23 Feb 2022 · FDA Enforcement Report

Enoki Mushrooms, brand Xuerong recalled by Golden Medal Mushroom

Golden Medal Mushroom is recalling Enoki Mushrooms, brand Xuerong, distributed in Illinois. The recall was initiated on 4 Feb 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codeslot # 300511
Quantity recalled36 cartons

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-0738-2022
FDA event ID
89540
Recalling firm
Golden Medal Mushroom, Commerce, CA
Brand
Enoki
Classification
Class I
Status
Terminated
Recall initiated
4 Feb 2022
FDA classified
16 Feb 2022
Reported
23 Feb 2022
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Listeria
Product category
Fish

Timeline

4 Feb 2022Recall initiated by company
16 Feb 2022Classified by FDA+12 days
23 Feb 2022Published in enforcement report+7 days

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

Reason for recall

Michigan Department of Agriculture and Rural Development sampled product and Listeria monocytogenes was detected.

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 Mushrooms, brand Xuerong, net wt. 200g/7.05-ounce packages, UPC 6 953150 100684. Product sent to distributor is packaged in a brown cardboard master case. The product name "ENOKI MUSHROOM" and other information in Chinese are printed in green color. The code "300511" is printed in blue color.

Where it was distributed

Distributed in IL.

Illinois

Questions about this recall

Why was it recalled?

Michigan Department of Agriculture and Rural Development sampled product and Listeria monocytogenes was detected.

Which lots are affected?

lot # 300511

Where was it sold?

Distributed in IL.

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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