UPC 24144500000 Ready Meals PEANUT BUTTER CHOCOLATE CHIP BAR With…
Reason Contains statement does not declare Almond
Milk Chocolate Catalog # 111 recall
Recalled by Giannios Candy Co Inc · Struthers, OH, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
This product is being recalled because it was manufactured using peanut butter recalled by Peanut Corporation of America because it has the potential to be contaminated with Salmonella
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
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
Milk Chocolate Catalog # 111, Dark Chocolate Peanut Clusters Catalog # 112 & Peanut Butter Pieces Catalog # 107 individually wrapped. Date Codes 121401-130831
Quantity: 5,090 boxes/250 pieces
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.
Peanut Butter Pieces Catalog #107, Milk Chocolate Clusters Catalog #111 & Dark Chocolate Clusters Catalog #112 Date Codes 121401-130831
Where it was sold
Michigan New York Ohio Pennsylvania
FDA's distribution note: The product was distributed in the states of OH, PA, MI, NY.
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
- Giannios Candy Co Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 6, 2009
- In FDA report of
- Mar 13, 2013
- Terminated
- Mar 1, 2013
- FDA recall number
- F-1031-2013 · event 51893
- Official record
- FDA enforcement report search
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