RecallHawk
Class I Recall

SSS brand and K-Fresh branded Enoki Mushrooms Packaged in clear plastic 200g container

LLK TRADING INC

Summary

The FDA issued a Class I for SSS brand and K-Fresh branded Enoki Mushrooms Packaged in clear plastic 200g con by LLK TRADING INC. Reason: Xin Ao International Group Corp, 601 E. Linden Ave Linden NJ 07036is initiating a recall of Enoki Mushroom, 200g, Plastic Bag, 25 bags per case becaus.

Details

Source

Food Recall

External ID

F-0651-2023

Action Date

2023-04-05

Status

Terminated

Category

food

Product Description

SSS brand and K-Fresh branded Enoki Mushrooms Packaged in clear plastic 200g container

Lot/Code Info: 6953150100677 expiration date of 02/15/2023

Quantity Affected: 400 cases

Reason for Recall

Xin Ao International Group Corp, 601 E. Linden Ave Linden NJ 07036is initiating a recall of Enoki Mushroom, 200g, Plastic Bag, 25 bags per case because the product may be contaminated with Listeria monocytogenes.

Distribution

The product was distributed to one firm in New York.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-01-28

Company

LLK TRADING INC

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 66 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 "F-0651-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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