Day Break Peanut Butter Fudge Crisp Bar 6x5
Recalling firm: Atkins Nutritionals, Inc.
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 13, 2017.
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637480055024, 637480059022FDA 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
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Full FDA record and distribution details
Original product description
Day Break Peanut Butter Fudge Crisp Bar 6x5, UPC: 637480055024, Case UPC: 637480059022. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 637480055024 | Day Break Peanut Butter Fudge Crisp Bar 6x5, UPC: 637480055024, Case UPC: 637480059022. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage |
| UPC | 637480059022 | Day Break Peanut Butter Fudge Crisp Bar 6x5, UPC: 637480055024, Case UPC: 637480059022. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage |
| best by | 10/1/2016 | 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 |
| best by | 4/29/2017 | t 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 by | 4/30/2017 | t K52742, Best By 10/1/2016; Lot K61192, Best By 4/29/2017; Lot K61202, Best By 4/30/2017 |
| best by | 9/30/2016 | 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 |
Original FDA recall reason
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.
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.
Data updated September 16, 2026. View official FDA data ↗
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