Golden Medal Enoki Mushrooms Recall: Listeria Contamination Risk
Golden Medal Mushroom Inc. recalls Enoki mushrooms from Korea with Listeria monocytogenes found in samples. Consumers should check UPC 809165 582015 for affected products.
Lower-risk recall
Michigan Department of Agriculture and Rural Development sampled product and results found Listeria monocytogenes.
Contact the company
What happened, in plain English
Golden Medal Mushroom Inc. is recalling Enoki mushrooms from Korea due to Listeria monocytogenes contamination detected in samples. This poses a risk of serious illness, especially for vulnerable populations like pregnant women and young children. Read more at govinfonow.com/recall/14667-golden-medal-enoki-mushrooms-recall-listeria-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/14667-golden-medal-enoki-mushrooms-recall-listeria-contamination-risk · Updated October 4, 2026 · FDA enforcement record: FDA #F-0471-2021
Cite this page
“Golden Medal Enoki Mushrooms Recall: Listeria Contamination Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14667-golden-medal-enoki-mushrooms-recall-listeria-contamination-risk. Based on FDA recall #F-0471-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0471-2021%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacteria that can cause serious infections, particularly in pregnant women, newborns, and people with weakened immune systems. The contamination was found in samples from the recalled mushrooms.
Who’s affected
This recall affects consumers who purchased the Enoki mushrooms with UPC 809165 582015 from Golden Medal Mushroom Inc. Pregnant women, newborns, and those with weakened immune systems are at higher risk of serious illness from Listeria.
How to tell if you have this one
Check for the UPC code 809165 582015 on the product label. The mushrooms come in a clear plastic bag with a green band across the bottom of the bag.
- Brand
Golden Medal Mushroom- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 809165 582015 on the product label to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- 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-0471-2021 (April 22, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0471-2021 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.