Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 3, 2022 (4 years ago)

Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in recall

Recalled by Nestle-USA, Inc. (Corporate Office) · Arlington, VA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potential of foreign material within product.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

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

Quantity: 18,671 cases

Food: Chocolate & candy Bread & bakery

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Alabama Arkansas Arizona California Colorado Connecticut District of Columbia Florida Georgia Illinois Indiana Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi North Carolina North Dakota Nebraska New Jersey Ohio Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wisconsin Wyoming

FDA's distribution note: 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

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Nestle-USA, Inc. (Corporate Office)
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 3, 2022
In FDA report of
Dec 14, 2022
Terminated
Mar 29, 2023
FDA recall number
F-0184-2023 · event 91115
Official record
FDA enforcement report search

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