Class ITerminated in FDA datasetJun 3, 2016

Day Break Peanut Butter Fudge Crisp Bar 6x5

Recalling firm: Atkins Nutritionals, Inc.

Why it was recalled

Atkins Nutritionals is recalling certain bar products because they contain or may have come in contact with equipment that processed product containing sunflower seeds distributed by supplier SunOpta Inc. that have the potential to be contaminated with Listeria monocytogenes.

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The exact product

Day Break Peanut Butter Fudge Crisp Bar 6x5, UPC: 637480055024, Case UPC: 637480059022. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Lot K52732, Best By 9/30/2016; Lot K52742, Best By 10/1/2016; Lot K61192, Best By 4/29/2017; Lot K61202, Best By 4/30/2017

TypeCode / valueContext
UPC637480055024Day Break Peanut Butter Fudge Crisp Bar 6x5, UPC: 637480055024, Case UPC: 637480059022. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
UPC637480059022Day Break Peanut Butter Fudge Crisp Bar 6x5, UPC: 637480055024, Case UPC: 637480059022. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
best by10/1/2016Lot K52732, Best By 9/30/2016; Lot K52742, Best By 10/1/2016; Lot K61192, Best By 4/29/2017; Lot K61202, Best By 4/30/2017
best by4/29/2017t K52732, Best By 9/30/2016; Lot K52742, Best By 10/1/2016; Lot K61192, Best By 4/29/2017; Lot K61202, Best By 4/30/2017
best by4/30/2017t K52742, Best By 10/1/2016; Lot K61192, Best By 4/29/2017; Lot K61202, Best By 4/30/2017
best by9/30/2016Lot K52732, Best By 9/30/2016; Lot K52742, Best By 10/1/2016; Lot K61192, Best By 4/29/2017; Lot K61202, Best By 4/30/2017

Recall details

Recall number
F-1715-2016
Event ID
74340
FDA status
Terminated
Initiated
Jun 3, 2016
Reported
Jul 27, 2016
Classified
Jul 18, 2016
Terminated
Feb 13, 2017
Quantity
19,913 cases
Location
Denver, CO, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide. Canadian and foreign consignees. No VA/govt/military.

FDA source record · F-1715-2016

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.