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.

Class I - Dangerous
Recalled: July 31, 2015 Kraft Heinz Foods Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    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
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Kraft Heinz Foods
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full 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.

Product Codes/Lot Numbers:

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

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2954-2015

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