CLASS I Food recall · Reported 30 Jul 2025 · FDA Enforcement Report

Needle Mushrooms recalled by Llk Trading

Llk Trading is recalling Needle Mushrooms, distributed in New York. The recall was initiated on 16 Jun 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesN/A
Quantity recalled80 Cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0337-2025
FDA event ID
97257
Recalling firm
Llk Trading, Linden, NJ
Brand
Needle
Classification
Class I
Status
Completed
Recall initiated
16 Jun 2025
FDA classified
25 Jul 2025
Reported
30 Jul 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Foreign Material
Product category
Mushrooms

Timeline

16 Jun 2025Recall initiated by company
25 Jul 2025Classified by FDA+39 days
30 Jul 2025Published in enforcement report+5 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product tested positive for L. monocytogenes .

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

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

Where it was distributed

The firms recalled product was distributed to the following State: NY

New York

Questions about this recall

Why was it recalled?

Product tested positive for L. monocytogenes .

Which lots are affected?

N/A

Where was it sold?

The firms recalled product was distributed to the following State: NY

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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