FDA recall record

Chocolate Covered Coconut Balls is packaged in either 2-ounce recall — FDA F-0940-2013

There is a potential of cross contamination with peanuts. The Chocolate Covered Coconut Balls were dipped in the same pot of melting chocolate that was…

Class IIclassification
F-0940-2013official record ID
Feb 6, 2013report date

Recall record at a glance

Official recordF-0940-2013
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmChocolate Decadence
Report dateFeb 6, 2013
Recall initiation dateDec 26, 2012
Quantity46/2 oz. packages; 5/1 lb. boxes; and 2/0.5 lbs boxes
LocationEugene, OR, United States

Official product description

Chocolate Covered Coconut Balls is packaged in either 2-ounce packages (2 pieces per package) or in 0.5 lb and 1 lb. boxes. The 2-ounce package has a UPC 19815 90007 8. There is no UPC for 0.5 lb. and 1 lb. packages. The product is labeled in parts: "***Chocolate Covered Coconut Balls***CHOCOLATE DECADENCE***Net Wt. 2oz (56.7g)***INGREDIENTS: Semi-sweet chocolate (sugar,

Why the product was recalled

There is a potential of cross contamination with peanuts. The Chocolate Covered Coconut Balls were dipped in the same pot of melting chocolate that was used to make product containing peanut butter.

Distribution information

Product was distributed in Arkansas California, Florida, Georgia, Indiana, Michigan, Minnesota, New Hampshire, New Jersey, New Mexico, New York, Oregon, Virginia, Washington, West Virginia, Wisconsin,

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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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