🔍 RecallPedia

Kashi Whole Grain Trail Mix Bars 35 g individual bar, 6 count retail carton (210 g), 12 cartons per case

Class I - Dangerous
Recalled: May 31, 2016 Kellogg Company Other Foods Nationwide

What Should You Do?

  1. Check if you have this product:
    6 count retail carton UPC 18627 43610 individual bar UPC 18627 43611 Better If Used Before Date/Best If Used By Date: 2017 JA 04 RE 2017 JA 05 RE 2017 JA 06 RE 2017 FE 10 RE
  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:
Kellogg Company
Reason for Recall:
Product contains sunflower seeds potentially contaminated with Listeria monocytogenes. Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Kashi Whole Grain Trail Mix Bars 35 g individual bar, 6 count retail carton (210 g), 12 cartons per case

Product Codes/Lot Numbers:

6 count retail carton UPC 18627 43610 individual bar UPC 18627 43611 Better If Used Before Date/Best If Used By Date: 2017 JA 04 RE 2017 JA 05 RE 2017 JA 06 RE 2017 FE 10 RE

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1755-2016

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