Food Recall Check
Class I · High risk Terminated Initiated Nov 24, 2014 (12 years ago)

Private Selection Extreme Moose Tracks Ice Cream 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

The ice cream product may contain peanuts not listed on the ingredient statement.

Undeclared allergen: Peanut

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Private Selection Extreme Moose Tracks Ice Cream; packaged in plastic 48 fl oz containers, UPC Code: 11110-00456

Quantity: 2282 cases, 6-48 fl oz cartons/case

Food: Ice cream

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.

APR 16 2015

Where it was sold

Alaska California Colorado Idaho Kansas Missouri Montana Nebraska Nevada Oregon Utah Washington Wyoming

FDA's distribution note: The affected product was distributed to domestic Kroger-owned stores in the following states: Alaska, California, Colorado, Idaho, Kansas, Missouri, Montana, Nebraska, Nevada, Oregon, Utah, Washington, Wyoming.

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. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. 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
Nov 24, 2014
In FDA report of
Dec 31, 2014
Terminated
Jun 29, 2015
FDA recall number
F-0752-2015 · event 69869
Official record
FDA enforcement report search

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