Food Recall Check
Class I · High risk Terminated Initiated Nov 12, 2012 (14 years ago)

Publix 7 Chocolate Split Layers recall

Recalled by Maplehurst Deli-Bake South Inc · Carrollton, GA, United States

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

Why it was recalled

Product sample was found to be positive for 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

Publix 7 Chocolate Split Layers, Net Wt. 12.75 lbs. (24 count), frozen in bulk paper cartons to be frosted and sold individually at the retail stores.

Food: Chocolate & candy

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 numbers: 2311B00610, 2311B00611, 23110C00611, Lot 231C00610 and 2311A00611.

Where it was sold

Florida Georgia

FDA's distribution note: FL & GA

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
Maplehurst Deli-Bake South Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 12, 2012
In FDA report of
Jan 16, 2013
Terminated
Feb 19, 2013
FDA recall number
F-0872-2013 · event 63735
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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