Class IOngoingVoluntary: Firm initiated
IQ PRODUCE, LLC: food recall H-0898-2026
IQ PRODUCE, LLC of Vernon, CA recalled Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286. Reason: Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes. The FDA listed it as Class I in its Enforcement Report dated Jun 10, 2026; distribution: California.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286
- Product quantity
- 319 units
- Reason for recall
- Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
- Codes, lots and dates on the package
- Lot UI775
- Distribution pattern
- Product was distributed to 3 California customers.
- Recalling firm
- IQ PRODUCE, LLC, Vernon, CA
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 14, 2026 |
| Classified by the FDA | Jun 2, 2026 |
| Published in the Enforcement Report | Jun 10, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0898-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.