FDA recall record

IQ PRODUCE Enoki Mushroom, Net Weight 150g recall — FDA H-0898-2026

Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.

Class Iclassification
H-0898-2026official record ID
Jun 10, 2026report date

Recall record at a glance

Official recordH-0898-2026
CategoryFood Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmIQ PRODUCE, LLC
Report dateJun 10, 2026
Recall initiation dateMay 14, 2026
Quantity319 units
LocationVernon, CA, United States

Official product description

Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286

Why the product was recalled

Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.

Distribution information

Product was distributed to 3 California customers.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.