RecallHawk
Class II Recall

Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case

Nestle-USA, Inc. (Corporate Office)

Summary

The FDA issued a Class II for Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 t by Nestle-USA, Inc. (Corporate Office). Reason: Potential of foreign material within product..

Details

Source

Food Recall

External ID

F-0184-2023

Action Date

2022-12-14

Status

Terminated

Category

food

Product Description

Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case

Lot/Code Info: Batch Numbers: 22135554RR, 22145554RR, 22155554RR Product Number: 12475670 Best By: 01/28/23 through 01/20/23

Quantity Affected: 18,671 cases

Reason for Recall

Potential of foreign material within product.

Distribution

AL, AR, AZ, CA, CO, CT, DC, FL, GA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NJ, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY

Type: Voluntary: Firm initiated

Recall Initiated: 2022-11-03

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 16 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-0184-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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