Diced and sliced yellow onions
Reason The firm was notified by a customer that the whole uncut product test positive for Listeria
Club Chef Broccoli & Raisin Salad Kits 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 their supplier that the product may be contaminated with 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
Club Chef Broccoli & Raisin Salad Kits, in 7.625 lb cases, containing 1bag (4.8 oz) of Raisin Sunflower Mix per case.
Quantity: 5,090 cases
Food: Leafy greens & salads
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.
Item #48001; Case Lot # 6127KT5 Use By: MAY-16-16; Packaging Lot #16089 3/29/16 & Lot number: 16123 Pack on date 4/28/16
Where it was sold
Georgia Indiana
FDA's distribution note: Product was shipped to GA & IN
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
- May 5, 2016
- In FDA report of
- Dec 14, 2016
- Terminated
- Jan 12, 2017
- FDA recall number
- F-0589-2017 · event 74066
- Official record
- FDA enforcement report search
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