Edible Cookie Dough Chocolate Chip packaged in 6 oz plastic cups lot # 3240
Summary
The FDA issued a Class I for Edible Cookie Dough Chocolate Chip packaged in 6 oz plastic cups lot # 3240 by Cookies-n-Milk Incorporated. Reason: Undeclared Peanut Butter; Packaged Peanut Butter Dough in Chocolate Chip packaging..
Details
Source
Food Recall
External ID
F-0325-2024
Action Date
2023-11-15
Status
Terminated
Category
food
Product Description
Edible Cookie Dough Chocolate Chip packaged in 6 oz plastic cups lot # 3240
Lot/Code Info: lot # 32402342 C
Quantity Affected: 2354 cases
Reason for Recall
Undeclared Peanut Butter; Packaged Peanut Butter Dough in Chocolate Chip packaging.
Distribution
Product is sold retail in Convenience stores in IA, KS, MN, MO, ND, NE, SD, WI, WY.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-27
Company
Mckinney, TX
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Cookies-n-Milk Incorporated) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cookies-n-Milk Incorporated have FDA actions?
This is the only FDA action we have on record for Cookies-n-Milk Incorporated in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0325-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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