Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 10, 2023 (3 years ago)

Nestle Toll House 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 presence of wood fragments.

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, 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

Quantity: 12,318 total cases (147,816 total packages) (12 cases destroyed due to warehouse damage at Nestle USA controlled DC)

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: 311457531K and 311557534K Best By Dates: 8/22/23 and 10/23/23

Where it was sold

Alabama Arizona California Colorado Florida Iowa Illinois Indiana Kansas Kentucky Louisiana Maine Michigan Minnesota Missouri Mississippi North Carolina Nebraska New Hampshire New York Ohio Oklahoma Pennsylvania Tennessee Texas Utah Virginia Wisconsin

FDA's distribution note: 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

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
Aug 10, 2023
In FDA report of
Sep 13, 2023
Terminated
Feb 9, 2024
FDA recall number
F-1491-2023 · event 92869
Official record
FDA enforcement report search

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