Food Recall Check
Class I · High risk Terminated Initiated Aug 5, 2020 (6 years ago)

MURRAY'S BACON CHIVE JARLSBERG DIP in plastic tubs 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

Potential contamination with Salmonella Newport.

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

MURRAY'S BACON CHIVE JARLSBERG DIP in plastic tubs, all sizes.

Quantity: 1,088 units

Food: Sauces, dips & dressings

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.

UPC: 207182-00000 Sell by dates: 5/22/20 through 8/13/20

Where it was sold

Alaska Arkansas Arizona Idaho Kentucky Louisiana Missouri Mississippi Montana New Mexico Nevada Ohio Oregon Tennessee Texas Utah Virginia Washington West Virginia Wyoming

FDA's distribution note: Products were distributed in the following states: AK, AZ, AR, ID, KY, LA, MS, MO, MT, NV, NM, OH, OR, TN, TX, UT, VA, WA, WV, & WY.

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
Aug 5, 2020
In FDA report of
Aug 26, 2020
Terminated
Sep 28, 2020
FDA recall number
F-1278-2020 · event 86203
Official record
FDA enforcement report search

Also recalled with it (16 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Showing 12 of 16.

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