Fresh Enoki Mushrooms 5.25oz/150 g/ 34 packages per case UPC: 001958939091 Distributed by Concord Farms, Vernon,
Summary
The FDA issued a Class I for Fresh Enoki Mushrooms 5.25oz/150 g/ 34 packages per case UPC: 001958939091 by Concord Farms, Inc.. Reason: California Department of Public Health sampled product and found it to contain Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0826-2022
Action Date
2022-03-16
Status
Terminated
Category
food
Product Description
Fresh Enoki Mushrooms 5.25oz/150 g/ 34 packages per case UPC: 001958939091 Distributed by Concord Farms, Vernon, CA Do not eat raw.
Lot/Code Info: No codes on package
Quantity Affected: 800
Reason for Recall
California Department of Public Health sampled product and found it to contain Listeria monocytogenes.
Distribution
CA, NV
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-09
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 92 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 (Concord Farms, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Concord Farms, Inc. have FDA actions?
This is the only FDA action we have on record for Concord Farms, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0826-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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