Utopia brand Enoki Mushroom; Utopia Foods Inc; 200g; Product of China; Distributed by Utopia Foods Inc.; UPC 89289186101
Summary
The FDA issued a Class I for Utopia brand Enoki Mushroom; Utopia Foods Inc; 200g; Product of China; Distribut by UTOPIA FOODS INC. Reason: Product may be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0376-2023
Action Date
2023-02-15
Status
Terminated
Category
food
Product Description
Utopia brand Enoki Mushroom; Utopia Foods Inc; 200g; Product of China; Distributed by Utopia Foods Inc.; UPC 892891861017; packaged in blue and clear plastic bag
Lot/Code Info: UPC 892891861017 Distributed from 01/06/2023 to 01/13/2023
Quantity Affected: 1619 cases
Reason for Recall
Product may be contaminated with Listeria monocytogenes.
Distribution
New York and New Jersey
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-13
Company
Glendale, NY
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 30 food recalls issued in the same week, part of 204 food-related FDA actions this month.
UTOPIA FOODS 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 (UTOPIA FOODS INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does UTOPIA FOODS INC have FDA actions?
UTOPIA FOODS 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-0376-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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