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Stop using now Food recall · FDA · Published February 23, 2022

Xuerong Enoki Mushroom Recall: Listeria Risk

Golden Medal Mushroom Inc. recalls Xuerong brand Enoki Mushrooms due to possible Listeria monocytogenes contamination.

🇺🇸 FDA recall #F-0813-2022FoodXuerong ›
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Recalling firmGOLDEN MEDAL MUSHROOM INC2770 Vail Ave · Commerce, CA 90040-2612
✎ GovInfoNow plain-language explainer

Golden Medal Mushroom Inc. is recalling Xuerong brand Enoki Mushrooms because they may be contaminated with Listeria monocytogenes. The affected product is sold in 150 g packages with UPC 6953150110157 and lot number 300511. This recall affects approximately 88 cases distributed to California, Texas, and Illinois. Read more at govinfonow.com/recall/13269-xuerong-enoki-mushroom-recall-listeria-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/13269-xuerong-enoki-mushroom-recall-listeria-risk · Updated October 10, 2026 · FDA enforcement record: FDA #F-0813-2022

Cite this page

“Xuerong Enoki Mushroom Recall: Listeria Risk.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/13269-xuerong-enoki-mushroom-recall-listeria-risk. Based on FDA recall #F-0813-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0813-2022%22&limit=1).

The FDA announced on Feb. 23, 2022, that Golden Medal Mushroom Inc. is recalling Xuerong brand Enoki Mushrooms due to a potential Listeria monocytogenes contamination. The voluntary Class I recall affects 88 cases distributed in California, Texas, and Illinois.

How to tell if you have it

  • Brand: Xuerong
  • Product: Enoki Mushrooms
  • Net weight: 150 g/ 5.25200g/7.05-ounce packages
  • UPC: 6953150110157
  • Lot code: 300511

The hazard

The product may be contaminated with Listeria monocytogenes. The FDA classified this as a Class I recall, indicating a high risk of adverse health consequences.

Context

GovInfoNow's records show Golden Medal Mushroom Inc. has two other recalls on record since April 22, 2021. On Feb. 4, 2022, the company issued a recall for Enoki Mushrooms due to Listeria contamination risk after samples tested positive for the bacteria. Other recent recalls of similar products include HEMU Enoki Mushrooms Recall (April 2, 2026), HH Fresh Enoki Mushrooms Recall (May 11, 2026), and IQ Produce Enoki Mushrooms Recall (May 14, 2026).

How to tell if you have this one

Check your refrigerator for Xuerong brand Enoki Mushrooms in 150 g (7.05-ounce) packages. Look for UPC 6953150110157 and lot code 300511 on the packaging.

  • Brand
    Xuerong
  • Product
    Enoki Mushrooms, brand Xuerong, net wt. 150 g/ 5.25200g/7.05-ounce packages, UPC 6953150110157. 34 0er carton
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled Enoki Mushrooms, even if cooked, as Listeria can survive some preparation methods.

  2. Discard or return the item

    Throw away the product or return it to the place of purchase for a refund.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “CA, TX, IL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Illinois, Texas.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Feb 23, 202212. FDA classified it Class I: Mar 3, 202223. Published in FDA’s Enforcement Report: Mar 9, 202234. FDA terminated the recall: Apr 25, 202242022
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0813-2022 (February 23, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0813-2022 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA