"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"
Summary
The FDA issued a Class II for "***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 by Nestle-USA, Inc. (Corporate Office). Reason: Consumer complaints reported presence of white pieces of plastic in cookie product..
Details
Source
Food Recall
External ID
F-0064-2023
Action Date
2022-10-26
Status
Terminated
Category
food
Product Description
"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"
Lot/Code Info: 21575554RR 21585554RR 21595554RR 21605554RR 21615554RR 21645554RR 21655554RR 21665554RR 21675554RR 21685554RR 21695554RR 21715554RR 21745554RR 21875554RR 21885554RR 21895554RR 21905554RR 21925554RR 21935554RR 21945554RR 22065554RR 22075554RR 22085554RR 22095554RR 22105554RR 22115554RR 22165554RR 22175554RR 22305554RR 22315554RR 22325554RR 22345554RR 22355554RR 22365554RR 22375554RR 22385554RR 22395554RR 22415554RR 22425554RR 22435554RR 22555554RR 22565554RR 22575554RR 22625554RR 22635554RR 22665554RR 22675554RR
Quantity Affected: 38,972 cases
Reason for Recall
Consumer complaints reported presence of white pieces of plastic in cookie product.
Distribution
AL, AR, AZ, CA, CO, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY and Puerto Rico
Type: Voluntary: Firm initiated
Recall Initiated: 2022-10-12
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 41 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-0064-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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