Publix 7 Chocolate Split Layers
Reason Product sample was found to be positive for Listeria monocytogenes.
Publix 7 Yellow Special Blend 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 Yellow Special Blend Layers, Net Wt. 14.25 lbs. (24 count), frozen in bulk paper cartons to be frosted and sold individually at the retail stores.
Quantity: 859 cases (24 units per case)
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-0871-2013 · 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.