Carton: Nabisco belVita Apple Cinnamon Net Wt. 8.8 oz UPC 0 44000 02824 1 Distributed by Kraft Foods Global, Inc. Northfield, IL 60093-2753 USA Inner Pouch: Nabisco belVita Apple Cinnamon Net Wt. 1.76 oz UPC 0 44000 02825 1 Distributed by Kraft Foods Global, Inc. Northfield, IL 60093-2753 USA Shipper: Mixed "Better For You" Shipper UPC 00044000034023 which also contains product not subject to the recall 590 cases distributed
Class I - DangerousWhat Should You Do?
- Check if you have this product: 8 Jan 12 through 2 Sep 13
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- Mondelez Global Llc
- Reason for Recall:
- Mondelez Global LLC is conducting a voluntary recall of belVita Breakfast Biscuit Apple Cinnamon and Chocolate Varieties due to the possible presence of fragments of flexible metal mesh caused by a faulty screen at third party flour supplier.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Carton: Nabisco belVita Apple Cinnamon Net Wt. 8.8 oz UPC 0 44000 02824 1 Distributed by Kraft Foods Global, Inc. Northfield, IL 60093-2753 USA Inner Pouch: Nabisco belVita Apple Cinnamon Net Wt. 1.76 oz UPC 0 44000 02825 1 Distributed by Kraft Foods Global, Inc. Northfield, IL 60093-2753 USA Shipper: Mixed "Better For You" Shipper UPC 00044000034023 which also contains product not subject to the recall 590 cases distributed
Product Codes/Lot Numbers:
8 Jan 12 through 2 Sep 13
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1069-2013
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