Nestle Toll House Valentine's Chocolate Chip cookie dough, Makes 20 cookies. Net wt 14 oz. UPC 0 28000-34408 5. Dist
Summary
The FDA issued a Class II for Nestle Toll House Valentine's Chocolate Chip cookie dough, Makes 20 cookies. Ne by Target Corporation. Reason: Improper storage temperature..
Details
Source
Food Recall
External ID
F-0535-2025
Action Date
2025-02-19
Status
Terminated
Category
food
Product Description
Nestle Toll House Valentine's Chocolate Chip cookie dough, Makes 20 cookies. Net wt 14 oz. UPC 0 28000-34408 5. Distributed by Nestle USA, Arlington, VA 22209.
Lot/Code Info: Best by 3/6/2025
Quantity Affected: 2904 each
Reason for Recall
Improper storage temperature.
Distribution
AK, CA, ID, MT, OR, WA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-14
Company
Minneapolis, MN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Target Corporation has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Target Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Target Corporation have FDA actions?
Target Corporation has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0535-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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