Lower riskFood recall · FDA · Published May 14, 2026
IQ Produce Enoki Mushrooms Recall: Listeria Contamination Risk
IQ Produce recalls 150g Enoki mushrooms from Korea due to Listeria Monocytogenes contamination. Consumers should avoid these products as they pose a food safety risk.
“IQ Produce Enoki Mushrooms Recall: Listeria Contamination Risk.” GovInfoNow, updated August 7, 2026. https://govinfonow.com/recall/6222-iq-produce-enoki-mushrooms-recall-listeria-contamination-risk. Based on FDA recall #H-0898-2026.
The FDA announced on May 14, 2026, that IQ PRODUCE, LLC is recalling Enoki Mushrooms due to Listeria Monocytogenes contamination. The agency stated the recall covers 319 units distributed to three California customers.
How to tell if you have it
Brand: IQ Produce
Product: Enoki Mushroom, Net Weight 150g; Product of Korea
UPC: 8809316 814286
Lot code: UI775
The hazard
Samples of the imported Enoki Mushrooms collected by the Florida Department of Health tested positive for Listeria Monocytogenes. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show IQ PRODUCE, LLC has one other recall on record since January 27, 2018, involving unapproved pesticide risk in Fresh Fragrant Pears. Other recent recalls of similar products include HEMU Enoki Mushrooms Recall (April 2, 2026), HH Fresh Enoki Mushrooms Recall (May 11, 2026), and CUISINE KETTLE Tomato Bisque Soup Kit Recall (August 11, 2026).
How to tell if you have this one
Check for the UPC 8809316 814286 on the packaging. The product is a 150g Enoki mushroom package from Korea distributed by IQ Produce.
Brand
IQ Produce
Product
Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286
Category
Food
Based on the official FDA remedy
What to do — step by step
Avoid Using Product
Do not consume or use the recalled Enoki mushrooms as they contain Listeria Monocytogenes.
Where it went and when
Where it was distributed
Distributed in California.
Listed by the agency
Not listed
FDA distribution: “Product was distributed to 3 California customers.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California.
Recall timeline
FDA published this recall 27 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-0898-2026 (May 14, 2026)
Plain-language summary written by qwen3:4b on August 7, 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.