Enoki Mushrooms 200g 50 units per box UPC: 851084 008358 Lot #3779 on outside of box Imported from Taiwan Distributor: J
Summary
The FDA issued a Class I for Enoki Mushrooms 200g 50 units per box UPC: 851084 008358 Lot #3779 on outside of by Jan Fruits, Inc.. Reason: Product found to contain Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0420-2023
Action Date
2023-03-22
Status
Terminated
Category
food
Product Description
Enoki Mushrooms 200g 50 units per box UPC: 851084 008358 Lot #3779 on outside of box Imported from Taiwan Distributor: Jan Fruits, Inc. 426 Charter Way Vernon, CA 90058
Lot/Code Info: Lot number 1101000673
Quantity Affected: 310 cases
Reason for Recall
Product found to contain Listeria monocytogenes
Distribution
Directly to California, then further distributed to Hawaii
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-24
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 488 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Jan Fruits, Inc. has 3 FDA actions in our database, including 3 recalls.
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 (Jan Fruits, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Jan Fruits, Inc. have FDA actions?
Jan Fruits, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0420-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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