Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286
Summary
The FDA issued a Class I for Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC by IQ PRODUCE, LLC. Reason: Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes..
Details
Source
Food Recall
External ID
H-0898-2026
Action Date
2026-06-10
Status
Ongoing
Category
food
Product Description
Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286
Lot/Code Info: Lot UI775
Quantity Affected: 319 units
Reason for Recall
Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
Distribution
Product was distributed to 3 California customers.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-14
Company
Vernon, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 166 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (IQ PRODUCE, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does IQ PRODUCE, LLC have FDA actions?
This is the only FDA action we have on record for IQ PRODUCE, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0898-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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