RecallHawk
Class I Recall

Enoki Mushrooms 200g 50 units per box UPC: 851084 008358 Lot #3779 on outside of box Imported from Taiwan Distributor: J

Jan Fruits, Inc.

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

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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