FDA Recall United States Terminated Historical recordClass III
IQ PRODUCE, LLC
- Product
- Fresh Fragrant Pear; Label - Double Trees Product of Chi…
- Published
- March 7, 2018
- Distribution
- CA
IQ PRODUCE, LLC Recall: Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
United States
OngoingClass I
- Company
- IQ PRODUCE, LLC
- Product
- Enoki Mushroom, Net Weight 150g; Product of Korea; Distribut…
- Recall date
- May 14, 2026
- Source
- FDA
Reason for recall
Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286 | 8809316 | 319 units | Lot UI775 |
Distribution
- Product was distributed to 3 California customers.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0898-2026
- Event ID
- 99001
- Status
- Ongoing
- Classification
- Class I
- Company
- IQ PRODUCE, LLC
- Product description
- Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286
- Quantity
- 319 units
- Reason
- Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
- Recall initiation date
- May 14, 2026
- Report date
- June 10, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Product was distributed to 3 California customers.
- UPC, lot, and code information
- UPC 8809316; Lot UI775
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: IQ PRODUCE, LLC
Other recalls from IQ PRODUCE, LLC
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
