Food Recall Check
Class I · High risk Terminated Initiated Dec 31, 2020 (6 years ago)

AF01886 NTFA No egg Ready-to-Eat Chocolate Chip Cookie Dough Dough recall

Recalled by Rhino Foods, Inc. · Burlington, VT, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Cookie dough ingredient intended for use in ice cream may be contaminated with Listeria monocytogenes.

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

AF01886 NTFA No egg Ready-to-Eat Chocolate Chip Cookie Dough Dough- 20 lb. sold frozen

Quantity: 3,280 20lb cases

Food: Chocolate & candy Bread & bakery Salads, sandwiches & prepared foods

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.

Lot/Unit Numbers: 3240 Expiration date(s) or Use by Date(s) or expected shelf life of product: 11/19/2021 Serial Numbers: n/a UPC Codes: 1 08 50908 00729 1

Where it was sold

Texas

FDA's distribution note: Texas - directly to manufacturer, none distributed into commerce

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Rhino Foods, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 31, 2020
In FDA report of
Jan 27, 2021
Terminated
Sep 8, 2021
FDA recall number
F-0215-2021 · event 87070
Official record
FDA enforcement report search

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