Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 30, 2017 (9 years ago)

All Natural Dark Chocolate Covered Coffee Beans INGREDIENTS 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

The products may contain an undeclared milk allergen.

Undeclared allergen: Milk

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

All Natural Dark Chocolate Covered Coffee Beans INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, CHOCOLATE LIQUOR PROCESSED WITH ALKALI, SOY LECITHIN (AN EMULSIFIER), VANILLA, SALT, AND ARTIFICIAL FLAVORING ADDED), DRY ROASTED COFFEE BEANS AND CONFECTIONERS GLAZE DIST BY THE KROGER CO CINCINNATI, OHIO 45201

Quantity: 2,641 pounds

Food: Chocolate & candy Juice & beverages

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.

PLU 54166 - All product purchased on or Before 10/30/2017

Where it was sold

Michigan

FDA's distribution note: Product was shipped to the state of MI.

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. The risk from an undeclared allergen is to people allergic to milk; 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
Oct 30, 2017
In FDA report of
Dec 27, 2017
Terminated
Jan 29, 2018
FDA recall number
F-0509-2018 · event 78421
Official record
FDA enforcement report search

Also recalled with it (5 more products)

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

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