Food Recall Check
Class I · High risk Terminated Initiated Sep 25, 2012 (14 years ago)

Moon Pie (R) Crunch Peanut Butter recall

Recalled by Chattanooga Bakery Inc · Chattanooga, TN, United States

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

Why it was recalled

Peanut Butter Crunch Moon Pies were manufactured with peanut butter supplied by Sunland, Inc. which was recall due to potential Salmonella contamination.

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

Moon Pie(R) Crunch Peanut Butter, CRUNCHY chocolate cookie sandwich, NET WT 2.4 oz and 9.6 oz , Baked by Chattanooga Bakery, Inc., Chattanooga, TN 37401

Quantity: 24,089 cases/1,090,752 units

Food: Peanut butter Chocolate & candy Bread & bakery Salads, sandwiches & prepared foods

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.

Best By dates: 02/26/13, 03/25/13, 04/29/13, 10/29/12, 12/10/12, 01/07/13, and 01/29/13 (UPC 072108089218 - 2.4 oz) (UPC 072108189017 - 9.6 oz)

Where it was sold

Nationwide.

FDA's distribution note: 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
Chattanooga Bakery Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 25, 2012
In FDA report of
Oct 31, 2012
Terminated
May 1, 2013
FDA recall number
F-0299-2013 · event 63271
Official record
FDA enforcement report search

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