Class IITerminated in FDA datasetJul 31, 2015

Kraft American Singles white American Pasteurized prepared cheese products packaged clear plastic. Sold at retail as 1lb. packages. Some products are only packaged in the clear plastic and…

Recalling firm: Kraft Heinz Foods

Why it was recalled

The Kraft American Singles Pasteurized prepared cheese products contain a thin strip of plastic film that may remain on the edge of some cheese slices after the wrapper is removed.

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The exact product

Kraft American Singles white American Pasteurized prepared cheese products packaged clear plastic. Sold at retail as 1lb. packages. Some products are only packaged in the clear plastic and some are packaged in the clear plastic with a blue label attached with white, black, and blue lettering.

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Code dates: December 29, 2015 to January 4, 2016 UPC code for the 3 lb. case: 210006154700 UPC code for the 4 lb. case: 210006256000 UPC code for the 3 lb. packages: 0 2100061582 7 UPC code for the 4 lb. packages: 0 2100063448 4

Recall details

Recall number
F-2955-2015
Event ID
71852
FDA status
Terminated
Initiated
Jul 31, 2015
Reported
Aug 19, 2015
Classified
Aug 13, 2015
Terminated
Aug 28, 2018
Quantity
3,245 cases of the 3 lb. packages (3-1 lb. packages/case) and 3,689 cases of the 4 lb. packages(4-1 lb. package/case).
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

Product was distrubuted multiple whole sale stores throughout the country. A list of all stores has been attached and sent via email to CFSAN recalls.

FDA source record · F-2955-2015

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

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.