“HH Fresh Enoki Mushrooms Recall: Listeria Contamination Risk.” GovInfoNow, updated August 9, 2026. https://govinfonow.com/recall/6232-hh-fresh-enoki-mushrooms-recall-listeria-contamination-risk. Based on FDA recall #H-0939-2026.
HH Fresh Trading Corp. recalled HH Fresh branded Enoki Mushrooms due to potential Listeria monocytogenes contamination, the FDA announced on May 11, 2026. The voluntary Class I recall affects 120 cases distributed to a customer in Texas and as samples in Florida.
The imported Enoki Mushrooms tested positive for Listeria Monocytogenes. The FDA classified the recall as Class I, indicating a reasonable probability that the product will cause serious adverse health consequences or death.
Context
GovInfoNow's records show HH FRESH TRADING CORP has one other recall on record since Oct. 11, 2024, for Enoki Mushrooms due to potential Listeria contamination. Other recent recalls of similar products include HEMU Enoki Mushrooms Recall (April 2, 2026), IQ Produce Enoki Mushrooms Recall (May 14, 2026), and CUISINE KETTLE Tomato Bisque Soup Kit Recall (Aug. 11, 2026).
How to tell if you have this one
Check for the UPC code 4711498860002 on the packaging. The product is labeled as 'HH Fresh Trading Corp. (branded) ENOKI MUSHROOM; Premium Quality; Net WT/ Poids Net 150g(5.29oz)'.
Brand
HH Fresh
Product
HH Fresh Trading Corp. (branded) ENOKI MUSHROOM; Premium Quality; Net WT/ Poids Net 150g(5.29oz) Distributed by HH
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product UPC
Look for the UPC code 4711498860002 on the packaging to identify affected items.
Where it went and when
Where it was distributed
Distributed in Florida and Texas.
Listed by the agency
Not listed
FDA distribution: “Product was distributed to a single customer located in Texas. Product was further distributed as samples were collected in Florida.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Texas.
Recall timeline
FDA published this recall 37 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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 #H-0939-2026 (May 11, 2026)
Plain-language summary written by qwen3:4b on August 9, 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.