Club Chef Broccoli & Raisin Salad Kits
Reason The firm was notified by their supplier that the product may be contaminated with Listeria monocytogenes.
Diced and sliced yellow onions recall
Recalled by Club Chef LLC · Covington, KY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The firm was notified by a customer that the whole uncut product test positive for Listeria
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
Diced and sliced yellow onions. 2.5 lb & 5 lb clear plastic bags
Quantity: 4,445 cases
Food: Onions
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.
Use By date 6/8/16, 6/9/16, 6/10/16, 6/11/16, 6/12/16, 6/13/16 & 6/14/16 and Julian dates: 150, 151, 153 & 154
Where it was sold
Iowa Illinois Indiana Kentucky Michigan Minnesota Missouri North Carolina Nebraska New Jersey Ohio Pennsylvania South Carolina Tennessee Virginia Wisconsin West Virginia
FDA's distribution note: Product was shipped to the following states: IA, IL, IN, KY, MI, MN, MO, NC, NE, NJ, OH, PA, SC, TN, VA, WI & WV.
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
- Club Chef LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 7, 2016
- In FDA report of
- Aug 10, 2016
- Terminated
- Mar 30, 2017
- FDA recall number
- F-1860-2016 · event 74601
- Official record
- FDA enforcement report search
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