FDA recall record

Talenti I Chocolate Peanut Butter Cup Gelato recall — FDA F-1060-2013

Talenti Gelato is recalling Talenti Chocolate Peanut Butter Cup Gelato. The peanut butter used in this product has the potential to be contaminated with…

Class Iclassification
F-1060-2013official record ID
Mar 20, 2013report date

Recall record at a glance

Official recordF-1060-2013
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmTalenti I, LLC
Report dateMar 20, 2013
Recall initiation dateOct 5, 2012
Quantity66,041 cases of pint size and 837 cases of 5 Qts size
LocationDallas, TX, United States

Official product description

Chocolate Peanut Butter Cup Gelato. The product was distributed to retail stores throughout the United States between September 2011 and September 2012 and is packaged in clear, plastic One Pint (473ml) containers with UPC code 1 86852 00094 5 printed on the back of the container and "Best By" date range of 3/21/13 through 3/26/14 printed on the bottom of the container. The firm also sold the product in a 5 QT size with UPC code 1-8685200090-7 and best by range 03/21/13 through 03/26/2014.

Why the product was recalled

Talenti Gelato is recalling Talenti Chocolate Peanut Butter Cup Gelato. The peanut butter used in this product has the potential to be contaminated with Salmonella. Consumption of food contaminated with Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often expe

Distribution information

Nationwide

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: Letter.

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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