FDA recall record

Jeni's Splendid Ice Creams Cinderella Pumpkin Ice Cream Bucket , 371, Jeni's Splendid Ice recall — FDA F-3104-2015

Product may be contaminated with Listeria monocytogenes.

Class Iclassification
F-3104-2015official record ID
Sep 16, 2015report date

Recall record at a glance

Official recordF-3104-2015
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmJeni's Splendid Ice Creams LLC
Report dateSep 16, 2015
Recall initiation dateApr 22, 2015
QuantityApproximately 61,267 total units for all 3 gallon sized products (buckets). Approximately 15,045 total units for all half gallon sized products. Appro
LocationColumbus, OH, United States

Official product description

Cinderella Pumpkin Ice Cream Bucket , 371, Jeni's Splendid Ice Creams, LLC, 3 gallons, plastic bucket, individually packed, frozen. Cinderella Pumpkin Ice Cream Half Gallon, Jeni's Splendid Ice Creams, LLC, half gallon, plastic container, individually packed, frozen. Cinderella Pumpkin Ice Cream Pint Case, Jeni's Splendid Ice Creams, LLC, half gallon, plastic container, 4 half gallons per case, frozen. Cinderella Pumpkin Ice Cream Pint Case, 271, Jeni's Splendid Ice Creams, LLC, pint size, plastic container, 8 pints per case, frozen.

Why the product was recalled

Product may be contaminated with Listeria monocytogenes.

Distribution information

National: AZ, CA, CO, CT, DE, FL, GA, IA, IN, KY, NH, NY, OH, OR, PA, TX, WA & WI. International: None reported.

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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