PlainRecalls
CriticalClass ICompleted

FDA Food recall · Reported July 30, 2025

Needle Mushrooms, Product of China, 200 gram packages, Plastic clear packaging on top with blue on the bottom (non-transparent). 25 packages per box .

Product tested positive for L. monocytogenes .

Recall #
H-0337-2025
Affected scope
80 Cases
Initiated
June 16, 2025
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Llk Trading INC recalled Needle Mushrooms, Product of China, 200 gram packages, Plastic clear packaging on top wit… - a critical-severity action.

Needle Mushrooms, Product of China, 200 gram packages, Plastic clear packaging on top wit… was recalled by Llk Trading INC in July 30, 2025. Reason: Product tested positive for L. monocytogenes .. Check the official notice for the remedy. Verify recall #H-0337-2025 with the FDA Food before acting.

The recall

Llk Trading INC issued this critical-severity FDA Food recall-Product tested positive for L. monocytogenes ..

Critical
severity level
Class I
classification
July 30, 2025
reported

Sourced from official FDA Food enforcement records. Verify recall #H-0337-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Medical Devices recalls over time

Where this recall sits in its category - 41,021 medical devices recalls on record

01,0002,0003,0004,000 20052008201120142017202020232026 1,947
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

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 .

Reason for recall

Product tested positive for L. monocytogenes .

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Completed
Recall number H-0337-2025
Date reported July 30, 2025
Date initiated June 16, 2025
Recalling firm Llk Trading INC
Firm location Linden, NJ
Affected scope 80 Cases
Distribution The firms recalled product was distributed to the following State: NY

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (H-0337-2025) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting, recall details can be updated.
  • This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Needle Mushrooms, Product of China, 200 gram packages, Plastic clear packaging on top with blue on the bottom (non-transparent). 25 packages per box .. Recalled by Llk Trading INC. Units affected: 80 Cases.
Why was this product recalled?
Product tested positive for L. monocytogenes .
Which agency issued this recall?
This recall was issued by the FDA Food on July 30, 2025. Severity: Critical. Recall number: H-0337-2025.
Where was the recalled product distributed?
Distribution: The firms recalled product was distributed to the following State: NY.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar Medical Devices · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

Compare this recall with GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VS… → · All Medical Devices recalls

This recall: FDA Food, reported July 30, 2025. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026