Fresh Enoki Mushrooms
Reason California Department of Public Health sampled product and found it to contain Listeria monocytogenes.
Concord Farms Fresh Enoki Mushrooms recall
Recalled by Concord Farms · Vernon, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
California Department of Public Health sampled Concord Farms Enoki Mushrooms which were positive 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
Concord Farms Fresh Enoki Mushrooms; 5.25 oz. (150g) or 7 oz. (200g) packages UPC: 049995041049 and 04999504103 US Distributor: Concord Farms, Vernon, CA All Natural, Product of Korea Keep Refrigerated. Rinse and Cook before eating.
Quantity: 1000 units
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 Minnesota Nevada
FDA's distribution note: U.S. distribution to the following: CA, NV, MN 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 completed: 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
- Concord Farms
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 28, 2021
- In FDA report of
- Jun 30, 2021
- Terminated
- Aug 10, 2021
- FDA recall number
- F-0751-2021 · event 88017
- Official record
- FDA enforcement report search