(Principal Display) ENOKI MUSHROOM Champignons d'enoki Net Wt: 150g (5.3oz) in a clear plastic packaged. (Back Display)
Summary
The FDA issued a Class I for (Principal Display) ENOKI MUSHROOM Champignons d'enoki Net Wt: 150g (5.3oz) in a by Enoki King Mushroom Farm Inc.. Reason: The product was found to have Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0075-2025
Action Date
2024-11-06
Status
Terminated
Category
food
Product Description
(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
Lot/Code Info: 4877
Quantity Affected: 864 cases
Reason for Recall
The product was found to have Listeria monocytogenes
Distribution
CA, MD, NY, NJ, VA, MA, and NC
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-10
Company
Ventura, 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 42 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 (Enoki King Mushroom Farm Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Enoki King Mushroom Farm Inc. have FDA actions?
This is the only FDA action we have on record for Enoki King Mushroom Farm Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0075-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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