Smart Sense Fruit & Granola Trail Mix, Net WT 4.0 oz , UPC 8 83967 29091 8, Distributed by Kmart corporation, Hoffman Estates, Il 60179, Minneapolis, MN 55414.

Class I - Dangerous
Recalled: February 25, 2013 American Importing Co Produce

What Should You Do?

  1. Check if you have this product:
    Lot # Best By Date 9/10/2012 7/10/2013 10/16/2012 8/16/2013 10/23/2012 8/23/2013 11/5/2012 9/5/2013 12/3/2012 10/3/2013 1/3/2013 11/3/2013 1/4/2013 11/4/2013 1/22/2013 11/22/2013
  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:
American Importing Co, Inc
Reason for Recall:
American Importing Co., d/b/a Amport Foods is voluntarily recalling a limited number of packages of its Amport Foods 16 oz Vanilla Almond Granola because they may contain pliable metal wire mesh fragments from a defective flour sifter from a 3rd party vendor.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Smart Sense Fruit & Granola Trail Mix, Net WT 4.0 oz , UPC 8 83967 29091 8, Distributed by Kmart corporation, Hoffman Estates, Il 60179, Minneapolis, MN 55414.

Product Codes/Lot Numbers:

Lot # Best By Date 9/10/2012 7/10/2013 10/16/2012 8/16/2013 10/23/2012 8/23/2013 11/5/2012 9/5/2013 12/3/2012 10/3/2013 1/3/2013 11/3/2013 1/4/2013 11/4/2013 1/22/2013 11/22/2013

Distribution:

Distributed in: IL, IN, IA, KS, MN, NJ, NY, NC, OH, SC, TX, VT

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1729-2013

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