Nestlé USA Announces Voluntary Recall of Limited Quantity of Edible Chocolate Chip Cookie Dough Tubs from NESTLÉ® TOLL HOUSE® Due to Potential Presence of Foreign Material - 11/8/22
Company Announcement Date:
November 03, 2022
FDA Publish Date:
November 03, 2022
Product Type:
Food & Beverages
Reason for Announcement:
Potential for Soft Plastic Film
Company Name:
Nestle USA
Brand Name:
NESTLÉ® TOLL HOUSE®
Product Description:
Edible Chocolate Chip Cookie Dough
ARLINGTON, VA., November 3, 2022 — Nestlé USA is initiating a voluntary recall of a limited quantity of Edible Chocolate Chip Cookie Dough tubs from NESTLÉ® TOLL HOUSE® due to the potential presence of soft plastic film.
This voluntary recall is isolated to three batches of Edible Chocolate Chip Cookie Dough tubs from NESTLÉ® TOLL HOUSE® that were produced August 1-3, 2022. These products were distributed to retailers nationwide.
This recall does not involve any other NESTLÉ® TOLL HOUSE® products, including other varieties of Edible cookie dough or Ready-to-Bake cookie dough.
While no illnesses or injuries have been reported, we took action out of an abundance of caution after a small number of consumers contacted Nestlé USA about this issue.
| NESTLÉ® TOLL HOUSE® Edible Chocolate Chip Cookie Dough Tub – Product Packaging (See image below) |
Batch Codes: 22135554RR 22145554RR 22155554RR Corresponding Best By Dates: |
Consumers who may have purchased these three batch codes (22135554RR, 22145554RR, 22155554RR) of Edible Chocolate Chip Cookie Dough tubs from NESTLÉ® TOLL HOUSE® should not consume the product and should return the product to the retailer where it was purchased for a replacement or refund. For any further support needed, please contact Nestlé USA at (800) 681-1678 Monday-Friday from 9 a.m.-6 p.m. EST.
Nestlé recently initiated a separate and unrelated recall for NESTLÉ® TOLL HOUSE® Stuffed Chocolate Chip Cookie Dough with Fudge Filling. Following each instance, we took immediate action to address the specific issue. We work closely with our suppliers and factory teams to ensure that our products are safe and meet the expectations of our consumers.
We are working with the U.S. Food & Drug Administration (FDA) on this voluntary recall and will cooperate with them fully.
The quality, safety and integrity of our products remain our number one priority. We sincerely apologize for any inconvenience this action represents to both our consumers and retail customers.
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* We believe that none of the product being recalled were processed or offered through the national office
* We strongly encourage you to notify your agencies within one business day from receipt of this notice.
* ALL cased and uncased inventories, both at the member level and agency level, need to be checked. This product may have entered member and agency warehouses through salvage, local donations, TEFAP, local purchases, retail pickups, food drives, or other avenues.
* For additional local details, please contact the Health Department(s) for the area(s) your food bank serves.
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About Feeding America Recall Notices
The Feeding America national office issues notifications of all national Class I and II recalls–those involving a health hazard situation in which there is reasonable probability that eating the food will cause health problems or death–and other recalls that may affect the safety of food supplied to network members.
The national office strongly encourages all member product solicitors, operations managers, and others involved in food and grocery distribution to regularly consult resources provided by the United States Food and Drug Administration (FDA) at http://www.fda.gov/opacom/7alerts.html, and the United States Department of Agriculture (USDA) at http://www.fsis.usda.gov/Fsis_Recalls/index.asp. Additionally, members can often receive information on national, state, and local recalls by contacting their local health departments.
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