Needle Mushrooms, Product of China, 200 gram packages, Plastic clear packaging on top with blue on the bottom (non-trans
Summary
The FDA issued a Class I for Needle Mushrooms, Product of China, 200 gram packages, Plastic clear packaging o by LLK TRADING INC. Reason: Product tested positive for L. monocytogenes ..
Details
Source
Food Recall
External ID
H-0337-2025
Action Date
2025-07-30
Status
Completed
Category
food
Product Description
Needle Mushrooms, Product of China, 200 gram packages, Plastic clear packaging on top with blue on the bottom (non-transparent). 25 packages per box .
Lot/Code Info: N/A
Quantity Affected: 80 Cases
Reason for Recall
Product tested positive for L. monocytogenes .
Distribution
The firms recalled product was distributed to the following State: NY
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-16
Company
Linden, NJ
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 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
LLK TRADING INC 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 (LLK TRADING INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does LLK TRADING INC have FDA actions?
LLK TRADING INC 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 "H-0337-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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