FDA recall record

Talenti Gelato One Pint recall — FDA F-0003-2014

Product contains undeclared Allergen; Almonds.

Class IIclassification
F-0003-2014official record ID
Oct 23, 2013report date

Recall record at a glance

Official recordF-0003-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmTalenti Gelato
Report dateOct 23, 2013
Recall initiation dateSep 10, 2013
Quantity3,018 Cases/24,144 units
LocationMarietta, GA, United States

Official product description

Talenti German Chocolate Cake Gelato, One Pint (473 mL), Crafted By: Talenti, Marietta, GA 30062.

Why the product was recalled

Product contains undeclared Allergen; Almonds.

Distribution information

AZ, CO, CT, DE, GA, IA, IN, MA, MD, MN, MO, NC, NH, NY, PA, TX and WI.

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: 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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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