Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 24, 2012 (14 years ago)

Arnold's Candies Handmade Since 1953 www.arnoldscandies.com… recall

Recalled by Dauphin Holdings, Inc. DBA Arnolds Candies · Akron, OH, United States

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

Why it was recalled

The firm was notified by the New York State Department of Agriculture & Marketing, that they failed to include the colors Yellow #5 and Blue #1 on their label.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Arnold's Candies Handmade Since 1953 www.arnoldscandies.com Wintergreen Puffs***INGREDIENTS: Sugar, Cream of Tarter, Artificial Flavoring and Coloring WARNING: Manufactured in a facility that also handles peanuts NET WT 6 oz (170g) 0 73629 00308 0 931 High Grove Blvd Akron, OH 44312 Best By: 07/11/14(19)1 lot code 06282012

Quantity: 100 cases/24/6 oz bags

Food: Chocolate & candy

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 0 73629 00308 0; Best By: 07/11/14(19)1 lot code 06282012

Where it was sold

New York Ohio Pennsylvania

FDA's distribution note: Product was shipped to the following states: NY, OH & PA.

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
Dauphin Holdings, Inc. DBA Arnolds Candies
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 24, 2012
In FDA report of
Dec 26, 2012
Terminated
Jun 28, 2013
FDA recall number
F-0846-2013 · event 63881
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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