Yes! Enoki Mushrooms
Reason California Department of Public Health sampled product with a result of Listeria monocytogenes
Yes! Enoki Mushrooms recall
Recalled by T Fresh Company DBA Yes Produce · 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 product with a result of 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
Yes! Enoki Mushrooms; Pesticide Free Produce: Vacuumed packed. Product of China UPC: 825382736947 Net Wt 200g/7.05 oz Distributed by YES Produce City of Industry, CA 91746
Quantity: 526 cases, 49 units per case
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 packages; Lot code provided by manufacturer. Lot number 6021053 on box
Where it was sold
California Florida New York Texas
FDA's distribution note: CA, FL, TX, 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
- T Fresh Company DBA Yes Produce
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 20, 2022
- In FDA report of
- May 25, 2022
- Terminated
- Jul 1, 2022
- FDA recall number
- F-1069-2022 · event 90066
- Official record
- FDA enforcement report search