Food Recall Check
Class I · High risk Terminated Initiated May 28, 2021 (5 years ago)

Conah Organic Enoki Mushrooms recall

Recalled by Marquis Worldwide Specialty Inc · City Of Industry, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

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.

Quantity: 1,320 cases

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

No codes on product

Where it was sold

Arizona California Texas

FDA's distribution note: U.S. distribution to the following: CA, TX, and AZ. No foreign distribution.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Marquis Worldwide Specialty Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
May 28, 2021
In FDA report of
Jul 7, 2021
Terminated
Jul 23, 2021
FDA recall number
F-0749-2021 · event 88016
Official record
FDA enforcement report search