Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz. Cookie dough in bar form packaged in paperboard tray with plast
Summary
The FDA issued a Class II for Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz. Cookie dough in bar for by Nestle-USA, Inc. (Corporate Office). Reason: Potential presence of wood fragments..
Details
Source
Food Recall
External ID
F-1491-2023
Action Date
2023-09-13
Status
Terminated
Category
food
Product Description
Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz. Cookie dough in bar form packaged in paperboard tray with plastic overwrap, 12 packages per case, Keep Refrigerated
Lot/Code Info: Batch Numbers: 311457531K and 311557534K Best By Dates: 8/22/23 and 10/23/23
Quantity Affected: 12,318 total cases (147,816 total packages) (12 cases destroyed due to warehouse damage at Nestle USA controlled DC)
Reason for Recall
Potential presence of wood fragments.
Distribution
The recalled product was distributed to the following states: AZ,LA,NH,MN.KS,NE,MO,FL,CA,TX,VA,PA,ME,NC,NY,TX,KY,TN,IN,MI,UT,WI,OH,MN,CO,MI,IL,IA,KY,MS,AL,OK
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-10
Company
Arlington, VA
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 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Nestle-USA, Inc. (Corporate Office) has 8 FDA actions in our database, including 8 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 (Nestle-USA, Inc. (Corporate Office)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Nestle-USA, Inc. (Corporate Office) have FDA actions?
Nestle-USA, Inc. (Corporate Office) has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1491-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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