ENOKI MUSHROOM; 200g/package (25 packages/case); vacuum packed; refrigerated "***ENOKI MUSHROOM***Net WT***200g(1.05oz)
Summary
The FDA issued a Class I for ENOKI MUSHROOM; 200g/package (25 packages/case); vacuum packed; refrigerated "* by HH FRESH TRADING CORP. Reason: Potential contamination of Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0255-2025
Action Date
2024-12-11
Status
Terminated
Category
food
Product Description
ENOKI MUSHROOM; 200g/package (25 packages/case); vacuum packed; refrigerated "***ENOKI MUSHROOM***Net WT***200g(1.05oz)***To keep sealed & cold Product of Taiwan Distributed by: HH Fresh Trading Los Angeles CA 90063 Exported by JIA YANG INTERNATIONAL ENTERPRISES CO., LTD. Produced by: Green Farm No. 303, Shichang S. Rd., Xiluo Township, Yunlin County 648106, Taiwan***Not serving raw food. Please eat it fully cooked.***"
Lot/Code Info: No lot code information on product
Quantity Affected: 2100 cases (200g/package; 25 packages/case)
Reason for Recall
Potential contamination of Listeria monocytogenes
Distribution
Retail stores in West Virginia.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-11
Company
Los Angeles, 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 107 food recalls issued in the same week, part of 204 food-related FDA actions this month.
HH FRESH TRADING CORP has 2 FDA actions in our database, including 2 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 (HH FRESH TRADING CORP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does HH FRESH TRADING CORP have FDA actions?
HH FRESH TRADING CORP has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0255-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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