CLASS I Food recall · Reported 16 Jan 2013 · FDA Enforcement Report

Publix 7 Chocolate Split Layers recalled by Maplehurst Deli-Bake South

Maplehurst Deli-Bake South is recalling Publix 7 Chocolate Split Layers, distributed in Florida, Georgia. The recall was initiated on 12 Nov 2012 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot numbers: 2311B00610, 2311B00611, 23110C00611, Lot 231C00610 and 2311A00611.

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0872-2013
FDA event ID
63735
Recalling firm
Maplehurst Deli-Bake South, Carrollton, GA
Brand
Publix
Classification
Class I
Status
Terminated
Recall initiated
12 Nov 2012
FDA classified
8 Jan 2013
Reported
16 Jan 2013
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Chocolate

Timeline

12 Nov 2012Recall initiated by company
8 Jan 2013Classified by FDA+57 days
16 Jan 2013Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product sample was found to be positive for Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

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.

Where it was distributed

FL & GA

FloridaGeorgia

Stores named: Publix

Questions about this recall

Is Publix 7 Chocolate Split Layers recalled?

Yes. Maplehurst Deli-Bake South recalled Publix 7 Chocolate Split Layers on 12 Nov 2012. The recall is Class I and its status is Terminated. Recall number F-0872-2013.

Why was it recalled?

Product sample was found to be positive for Listeria monocytogenes.

Which lots are affected?

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

Where was it sold?

FL & GA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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