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Stop using now Food recall · FDA · Published May 28, 2021

Rainfield Enoki Mushrooms Contain Listeria - Do Not Consume

Rainfield Marketing Group recalls Enoki mushrooms with Listeria monocytogenes contamination. Do not consume these products from Korea with UPC 085412004020.

🇺🇸 FDA recall #F-0748-2021FoodRainfield Marketing Group ›
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Recalling firmRAINFIELD MARKETING GROUP3305 Bandini Blvd · Vernon, CA 90058-4130
✎ GovInfoNow plain-language explainer

Rainfield Marketing Group is recalling Enoki mushrooms that tested positive for Listeria monocytogenes. This bacteria can cause serious illness, so these products should not be eaten. Read more at govinfonow.com/recall/14471-rainfield-enoki-mushrooms-contain-listeria-do-not-consume.

Source Summary by GovInfoNow · govinfonow.com/recall/14471-rainfield-enoki-mushrooms-contain-listeria-do-not-consume · Updated October 4, 2026 · FDA enforcement record: FDA #F-0748-2021

Cite this page

“Rainfield Enoki Mushrooms Contain Listeria - Do Not Consume.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14471-rainfield-enoki-mushrooms-contain-listeria-do-not-consume. Based on FDA recall #F-0748-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0748-2021%22&limit=1).

The FDA announced on May 28, 2021, that Rainfield Marketing Group voluntarily recalled Enoki Mushroom products due to a positive result for Listeria monocytogenes. Consumers should not consume the product raw.

How to tell if you have it

  • Brand: Rainfield Marketing Group
  • Product: Enoki Mushroom, 150g clear plastic bag with orange bottom; UPC 085412004020 Product of Korea Do no consume Raw
  • UPC: 00085412004020

The hazard

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

Context

GovInfoNow's records show other recent recalls of similar products include HEMU Enoki Mushrooms Recall: Listeria Contamination Risk (2026-04-02), IQ Produce Enoki Mushrooms Recall: Listeria Contamination Risk (2026-05-14), and HH Fresh Enoki Mushrooms Recall: Listeria Contamination Risk (2026-05-11).

How to tell if you have this one

Look for Enoki mushrooms in 150g clear plastic bags with an orange bottom. The product has UPC 085412004020 and was made in Korea.

  • Brand
    Rainfield Marketing Group
  • Product
    Enoki Mushroom, 150g clear plastic bag with orange bottom; UPC 085412004020 Product of Korea Do no consume Raw
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Do not consume these Enoki mushrooms as they contain Listeria monocytogenes.

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: not listedILWisconsin: 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: yesMDDelaware: 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: “U.S. distribution to the following: CA, TX, MD No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Maryland, Texas.

Recall timeline

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

1. Firm started the recall: May 28, 202112. Published in FDA’s Enforcement Report: Jun 16, 202123. FDA classified it Class I: Jun 28, 202134. FDA terminated the recall: Aug 6, 202142021
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  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-0748-2021 (May 28, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0748-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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