FDA recall record

Giant Eagle Candy Place Chocolate Santas, in 11 oz clear plastic bags recall — FDA F-1438-2014

Giant Eagle Candy Place Chocolate Santas do not declare the peanut allergen ingredient on the primary package label. Also, the caramel variety ingredient…

Class Iclassification
F-1438-2014official record ID
Jan 29, 2014report date

Recall record at a glance

Official recordF-1438-2014
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmGiant Eagle
Report dateJan 29, 2014
Recall initiation dateDec 27, 2013
Quantity1372 units purchased by customers
LocationPittsburgh, PA, United States

Official product description

Candy Place Chocolate Santas, in 11 oz clear plastic bags, individually wrapped assortment of double chocolate, caramel, and peanut butter flavored chocolates, distributed by Giant Eagle, Pittsburgh, PA. Ingredients: Sugar, partially hydrogenated vegetable oil (Palm kernel, coconut, and/or palm), cocoa (processed with alkali) whey, lactose, skim milk, soy lecithin (emulsifier), vanillin (artificial flavor).

Why the product was recalled

Giant Eagle Candy Place Chocolate Santas do not declare the peanut allergen ingredient on the primary package label. Also, the caramel variety ingredient statement was not included in the finished product label.

Distribution information

Exclusively to Giant Eagle retail supermarkets in PA, OH, and MD.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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