Smoked Mozzarella Penne Salad
Reason Store-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes
Kroger Raw #4 Macadamia Nuts recall
Recalled by The Kroger Co · Cincinnati, OH, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Positive Salmonella sample results in Kroger brand raw Macadamia nuts
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
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
Kroger Raw #4 Macadamia Nuts. UPC 2 04192 51053 2 Dist. by the Kroger Company Cincinnati, Ohio 45202
Quantity: 28, 675 lbs in 25 lb packages
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.
SELL BY 10 14 15 #54192
Where it was sold
Alabama Arkansas Georgia Illinois Indiana Kansas Kentucky Louisiana Michigan Missouri Mississippi Nebraska Ohio South Carolina Tennessee Texas Virginia West Virginia
FDA's distribution note: Product was shipped to the following states:: AL, AR, GA, IL, IN, KS, KY, LA, MI, MO, MS, NE, OH, SC, TN, TX, VA & 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
- The Kroger Co
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 16, 2015
- In FDA report of
- May 11, 2016
- Terminated
- Aug 18, 2016
- FDA recall number
- F-1320-2016 · event 72417
- Official record
- FDA enforcement report search
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