CLASS I Food recall · Reported 9 Mar 2022 · FDA Enforcement Report

Enoki Mushrooms, brand Xuerong recalled by Golden Medal Mushroom

Golden Medal Mushroom is recalling Enoki Mushrooms, brand Xuerong, distributed in California, Illinois, Texas. The recall was initiated on 23 Feb 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 300511.
Quantity recalled88 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-0813-2022
FDA event ID
89668
Recalling firm
Golden Medal Mushroom, Commerce, CA
Brand
Enoki
Classification
Class I
Status
Terminated
Recall initiated
23 Feb 2022
FDA classified
3 Mar 2022
Reported
9 Mar 2022
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Listeria
Product category
Mushrooms

Timeline

23 Feb 2022Recall initiated by company
3 Mar 2022Classified by FDA+8 days
9 Mar 2022Published in enforcement report+6 days

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

Reason for recall

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 Mushrooms, brand Xuerong, net wt. 150 g/ 5.25200g/7.05-ounce packages, UPC 6953150110157. 34 0er carton.

Where it was distributed

CA, TX, IL

CaliforniaIllinoisTexas

Questions about this recall

Why was it recalled?

Listeria monocytogenes

Which lots are affected?

Lot 300511.

Where was it sold?

CA, TX, 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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