FDA recall record

Abdallah Candies Net Wt 4.5 oz recall — FDA F-0764-2015

Abdallah Candies is recalling red and silver foil wrapped Holiday Caramel Bites. One customer reported finding a Peanut Butter Bite wrapped in red foil in…

Class Iclassification
F-0764-2015official record ID
Jan 14, 2015report date

Recall record at a glance

Official recordF-0764-2015
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmAbdallah Candies, Inc.
Report dateJan 14, 2015
Recall initiation dateDec 4, 2014
Quantity330 cases of 6 bags each
LocationBurnsville, MN, United States

Official product description

Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate (sugar, chocolate liquor, cocoa butter, whole milk, soy lecithin (an emulsifier), vanilla), corn syrup, sweetened condensed milk, cream, sugar, palm oil, salt, guar gum. carrageenan, locust bean gum, potassium sorbate (preservative), artificial flavor. Share equipment with items that may contain peanuts, tree nuts, egg. CONTAINS MILK, SOY. GLUTEN FREE. The product is sold in a box of 6 cellophane bags with 8 bites in each bag. Four are wrapped in red and 4 in silver foil.

Why the product was recalled

Abdallah Candies is recalling red and silver foil wrapped Holiday Caramel Bites. One customer reported finding a Peanut Butter Bite wrapped in red foil in a bag of Holiday Caramel Bites.

Distribution information

AK, AZ, CA, CO, CT, DE, GA, ID, IL, IN, IA, KS, KY, LA, MA, MI, MN, MS, MO, MT ,NE, NV,NH, NH, NY, ND, OH, OK, PA, SC, SD, TN, VA, WA, WI, WY.

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: Telephone.

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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