Food Recall Check
Class I · High risk Terminated Initiated Mar 18, 2022 (5 years ago)

Top Quality Produce Enoki Mushrooms recall

Recalled by Top Quality Produce, Inc · Irwindale, CA, United States

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

Why it was recalled

California Department of Public Health tested Enoki mushrooms and had 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

Top Quality Produce Enoki Mushrooms; 200G/7.05 oz. clear package with green bottom. Vacuumed packed Product of Taiwan. Keep Refrigerated, Cook before Eating. UPC: 848180019661 50 bags per box Distributed by: Top Quality Produce, Inc., Irwindale, CA 91706

Quantity: 1108 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

California Colorado Minnesota New York Ohio Washington

FDA's distribution note: CA, OH, CO, MN, WA, NY

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
Top Quality Produce, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 18, 2022
In FDA report of
Apr 13, 2022
Terminated
May 19, 2022
FDA recall number
F-0964-2022 · event 89858
Official record
FDA enforcement report search