Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 24, 2013 (13 years ago)

Giant Eagle Candy Place Chocolate Covered Peanuts recall

Recalled by Giant Eagle · Pittsburgh, PA, United States

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

Why it was recalled

The firm has issued a recall on Giant Eagle Candy Place Chocolate Covered Peanuts with UPC 3003404313. The product has whey in the ingredients and the label does not clearly state that there is a milk allergen. (only whey is listed in the ingredient statement).

Undeclared allergens: Milk 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

Giant Eagle Candy Place Chocolate Covered Peanuts NET WT. 5 OZ, UPC code 3003404313 This product was packaged in a facility that also processes peanuts, nuts, milk products, soy, wheat, sesame seeds, whey and eggs. Distributed By: Giant Eagle, Inc. Pittsburgh, PA 15328-2809

Quantity: unknown

Food: Nuts & seeds 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.

All codes

Where it was sold

FDA's distribution note: Giant Eagle retail stores in 4 states.

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, 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
Giant Eagle
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 24, 2013
In FDA report of
Aug 14, 2013
Terminated
May 18, 2015
FDA recall number
F-1790-2013 · event 65801
Official record
FDA enforcement report search

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