Taiwan Best Quality Enoki Natural Mushrooms, Premium 200g/7.5 oz. clear plastic package. 50 pcs per box. Manufactu
Summary
The FDA issued a Class I for Taiwan Best Quality Enoki Natural Mushrooms, Premium 200g/7.5 oz. clear plasti by Jan Fruits, Inc.. Reason: California Department of Public Health sampled product and found it to contain Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0827-2022
Action Date
2022-03-16
Status
Terminated
Category
food
Product Description
Taiwan Best Quality Enoki Natural Mushrooms, Premium 200g/7.5 oz. clear plastic package. 50 pcs per box. Manufacturer: Changhua County Mushroom Production Cooperative; Distributed by Jan Fruits. UPC: 8 51084 00835 8
Lot/Code Info: No codes on product.
Quantity Affected: 617 cases
Reason for Recall
California Department of Public Health sampled product and found it to contain Listeria monocytogenes.
Distribution
One distributor in CA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-08
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.
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-0827-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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