Check the Batch
Class IIITerminated in FDA datasetAug 29, 2014

Individually 2/3 oz. slices of American cheese product individually wrapped in transparent plastic an packaged in 12 oz. and 16 oz.. packages, and 4 lb. cartons under the Kraft brand name.…

Recalling firm: Kraft Heinz Foods

Why it was recalled

Kraft Foods Group is voluntarily recalling 7,691 cases of select varieties of regular Kraft American Singles Pasteurized Prepared Cheese Product. A supplier did not store an ingredient used in this product in accordance with Kraft's temperature standards.

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Compare the exact product and package details with the label you have.

ProductIndividually 2/3 oz. slices of American cheese product individually wrapped in transparent plastic an packaged in 12 oz. and 16 oz.. packages, and 4 lb. cartons under the Kraft brand name. Cases of 12 oz. packages include 48 packages per case. Cases of 16 oz. packages include either 12 or 36 packages per case. Cases of 4 lb. cartons include 8 cartons per case.

FDA code information

1) 12 oz. packages of singles; UPC (Retail Package): 021000604647; Code Dates: 20 FEB 2015, 21 FEB 2015; UPC Code (Case): 210006046400; 2) 16 oz. packages of singles; UPC (Retail Package): 021000615261; Code Date: 20 FEB 2015; UPC Code (Case): 210006145000; 3) 16 oz. packages of singles; UPC (Retail Package): 021000615261; Code Date: 20 FEB 2015; UPC Code (Case): 210006152600; 4) 4 lb. cartons of singles; UPC (Retail Package): 021000633609; Code Date: 20 FEB 2015; UPC Code (Case): 210006255900

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Full FDA record and distribution details

Original product description

Individually 2/3 oz. slices of American cheese product individually wrapped in transparent plastic an packaged in 12 oz. and 16 oz.. packages, and 4 lb. cartons under the Kraft brand name. Cases of 12 oz. packages include 48 packages per case. Cases of 16 oz. packages include either 12 or 36 packages per case. Cases of 4 lb. cartons include 8 cartons per case.

Recall details

Recall number
F-0022-2015
Event ID
69142
FDA status
Terminated
Initiated
Aug 29, 2014
Reported
Oct 22, 2014
Classified
Oct 10, 2014
Terminated
Aug 8, 2016
Quantity
7,691 cases
Location
Northfield, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

US: Nationwide (AL, AR, CA, CA, FL, GA, IL, IN, KS, MI, NC, NJ, OH, OK, TN, TX, VA)

FDA source record · F-0022-2015

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.