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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food

Kraft Heinz Foods: 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.

Agency Publication Date: August 13, 2015
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Affected Products

Product: Kraft American Singles Pasteurized prepared cheese products packaged clear plastic. Sold at retail as 1 lb. 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.

Code dates: December 29, 2015 to January 4, 2016 UPC codes for the cases: 210006255900 and 210006152400 UPC code for the units: 0 2100063360 9 and 0 2100060491 3

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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.

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

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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 71852
Status: Resolved
Manufacturer: Kraft Heinz Foods
Manufactured In: United States
Units Affected: 2 products (1,1648 cases of the 4 lb. packages (4- 1 lb. packages/case) and 17,177 cases of the 3 lb. package.(3-1 lb. packages/case).; 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).)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.