Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 19, 2020 (7 years ago)

PRIVATE SELECTION FROZEN BERRY MEDLEY in recall

Recalled by The Kroger Co · Cincinnati, OH, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potential norovirus contamination.

Pathogen: Norovirus

A highly contagious virus, often linked to shellfish and fresh produce.

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

PRIVATE SELECTION FROZEN BERRY MEDLEY in 16 oz. (10 bags per case) and 48 oz. bags (6 bags per case). UPC: 0001111079120

Quantity: 8,499 total cases.

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.

16 oz. bags - BEST BY: 06/02/21 and 06/04/21 48 oz. bags - BEST BY: 06/02/21 and 06/03/21

Where it was sold

Alaska Alabama Arkansas Arizona California Colorado Georgia Idaho Illinois Indiana Kansas Kentucky Louisiana Michigan Missouri Mississippi Montana Nebraska New Mexico Nevada Ohio Oregon South Carolina Tennessee Texas Utah Virginia Washington Wisconsin West Virginia Wyoming

FDA's distribution note: Product was distributed to the following states: following states: AK, AL, AR, AZ, CA, CO, GA, ID, IL, IN, KS, KY, LA, MI, MO, MS, MT, NE, NM, NV, OH, OR, SC, TN, TX, UT, VA, WA, WI, WV, & WY.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
Mar 19, 2020
In FDA report of
Apr 15, 2020
Terminated
Aug 4, 2020
FDA recall number
F-0884-2020 · event 85276
Official record
FDA enforcement report search

Also recalled with it (1 more product)

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

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