Class ITerminatedVoluntary: Firm initiated
Enoki King Mushroom Farm Inc.: food recall F-0075-2025
Enoki King Mushroom Farm Inc. of Ventura, CA recalled (Principal Display) ENOKI MUSHROOM Champignons d'enoki Net Wt: 150g (5.3oz) in a clear plastic packaged. (Back… Reason: The product was found to have Listeria monocytogenes. The FDA listed it as Class I in its Enforcement Report dated Nov 6, 2024; distribution: California, Massachusetts, Maryland, North Carolina, New Jersey, New York, Virginia.
Record status as published: Terminated (terminated Dec 31, 2024). 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
- (Principal Display) ENOKI MUSHROOM Champignons d'enoki Net Wt: 150g (5.3oz) in a clear plastic packaged. (Back Display) UPC 860011505600 Keep Refrigerated Garder Au Froid Distributed by: Global Fresh Marketing Commerce, CA 90040
- Product quantity
- 864 cases
- Reason for recall
- The product was found to have Listeria monocytogenes
- Codes, lots and dates on the package
- 4877
- Distribution pattern
- CA, MD, NY, NJ, VA, MA, and NC
- Recalling firm
- Enoki King Mushroom Farm Inc., Ventura, 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
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Oct 10, 2024 |
| Classified by the FDA | Oct 29, 2024 |
| Published in the Enforcement Report | Nov 6, 2024 |
| Terminated | Dec 31, 2024 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0075-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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