RecallHawk
Class I Recall

Conah Organic Enoki Mushrooms; 200 g (7.05 oz.) clear package with orange bottom UPC 8 51511 00770 1 Distributed by:

Marquis Worldwide Specialty Inc

Summary

The FDA issued a Class I for Conah Organic Enoki Mushrooms; 200 g (7.05 oz.) clear package with orange botto by Marquis Worldwide Specialty Inc. Reason: California Department of Public Health sampled Conah Organic Enoki mushrooms with a positive result for Listeria monocytogenes..

Details

Source

Food Recall

External ID

F-0749-2021

Action Date

2021-07-07

Status

Terminated

Category

food

Product Description

Conah Organic Enoki Mushrooms; 200 g (7.05 oz.) clear package with orange bottom UPC 8 51511 00770 1 Distributed by: Marquis Worldwide Specialty Inc. City of Industry, CA 91748 Cook for a minimum of 7-8 mins before consumption.

Lot/Code Info: No codes on product

Quantity Affected: 1,320 cases

Reason for Recall

California Department of Public Health sampled Conah Organic Enoki mushrooms with a positive result for Listeria monocytogenes.

Distribution

U.S. distribution to the following: CA, TX, and AZ. No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-05-28

Company

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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (Marquis Worldwide Specialty Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Marquis Worldwide Specialty Inc have FDA actions?

This is the only FDA action we have on record for Marquis Worldwide Specialty Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0749-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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