Ultimate Chocolate Chip Cookie Dough Pie, refrigerated/frozen. A 9-inch pastry shell with a layer of chocolate chip cookie dough baked in the bottom followed by a layer of French silk. Finished with whipped cream, chocolate drizzle and chocolate chip cookie dough bites distributed across the top of pie. 39 oz.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Material #29578 and #29978 Batch Numbers: 2016188, 2016190, 2016193, 2016195, 2016197, 2016200, 2016202, 2016204, 2016207, 2016209, 2016211
  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 Blue Ribbon Holdings DBA Legendary Baking
Reason for Recall:
Product incorporated cookie dough that was potentially contaminated with Listeria Monocytogenes.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Ultimate Chocolate Chip Cookie Dough Pie, refrigerated/frozen. A 9-inch pastry shell with a layer of chocolate chip cookie dough baked in the bottom followed by a layer of French silk. Finished with whipped cream, chocolate drizzle and chocolate chip cookie dough bites distributed across the top of pie. 39 oz.

Product Codes/Lot Numbers:

Material #29578 and #29978 Batch Numbers: 2016188, 2016190, 2016193, 2016195, 2016197, 2016200, 2016202, 2016204, 2016207, 2016209, 2016211

Distribution:

Distributed in: IA, IL, IN, MN, WI, OH

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0687-2017

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