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Class II: temporary or reversible health riskTerminated

Kraft American Singles Pasteurized prepared Recall

Kraft American Singles Pasteurized prepared cheese products packaged clear plastic

Kraft Heinz Foods · Northfield, IL

Risk level
Class II
Reported by FDA
Aug 19, 2015
Recall ID
F-2954-2015
Check your lot numberHow we source this data

Summary

Kraft Heinz Foods recalled Kraft American Singles Pasteurized prepared starting Jul 31, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2954-2015 on Aug 19, 2015. Reason: 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. Status: Terminated.

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.

Product description

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.

Lot numbers, UPCs & expiration codes

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

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2954-2015
Classification
Class II
Status
Terminated
Recall initiated
Jul 31, 2015
FDA report date
Aug 19, 2015
Quantity
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).
Recall type
Voluntary: Firm initiated
Recalling firm
Kraft Heinz Foods

Original FDA data

Every field from FDA enforcement report F-2954-2015, exactly as published.

Show all FDA fields
City
Northfield
State
IL
Status
Terminated
Country
United States
Event ID
71852
Address
3 Lakes Dr
Code information
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
Postal code
60093-2753
Report date
Aug 19, 2015
Product type
Food
Recall number
F-2954-2015
Classification
Class II
Recalling firm
Kraft Heinz Foods
Product quantity
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).
Termination date
Aug 28, 2018
Reason for recall
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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.
Distribution pattern
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.
Recall initiation date
Jul 31, 2015
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Aug 13, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2954-2015, published Aug 19, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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