HH Fresh Trading Corp
Reason Imported Enoki Mushrooms tested positive for Listeria Monocytogenes.
Enoki Mushroom recall
Recalled by Hh Fresh Trading CORP · Los Angeles, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential contamination of Listeria monocytogenes
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
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.***"
Quantity: 2100 cases (200g/package; 25 packages/case)
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
No lot code information on product
Where it was sold
West Virginia
FDA's distribution note: Retail stores in West Virginia.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Hh Fresh Trading CORP
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 11, 2024
- In FDA report of
- Dec 11, 2024
- Terminated
- May 6, 2025
- FDA recall number
- F-0255-2025 · event 95637
- Official record
- FDA enforcement report search