Food Recall Check
Class I · High risk Terminated Initiated Jun 3, 2022 (4 years ago)

Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey Butter Cake recall

Recalled by Prairie City Bakery · Vernon Hills, IL, United States

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

Why it was recalled

Salmonella. Product contains recalled Jif peanut butter as ingredient.

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

Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey Butter Cake 2oz. individual UPC: 7-9788436718-2; 10 individual units per display unit; 6 display units per wholesale case.

Quantity: 626 cases

Food: Milk & dairy Peanut butter Chocolate & candy Bread & bakery

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.

1357-1: Best by 6/23/2023 and 2085-1: Best by: 9/25/2023

Where it was sold

Nationwide.

FDA's distribution note: sold at gas stations and convenience stores nationwide

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
Prairie City Bakery
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 3, 2022
In FDA report of
Jul 13, 2022
Terminated
Nov 9, 2023
FDA recall number
F-1402-2022 · event 90416
Official record
FDA enforcement report search

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