Day Break Chocolate Hazelnut 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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637480055321, 637480059534FDA code information
Lot K52964, Best By 10/23/2016; Lot K53504, Best By 12/16/2016; Lot K53514, Best By 12/17/2016; Lot K53524, Best By 12/18/2016
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Full FDA record and distribution details
Original product description
Day Break Chocolate Hazelnut Bar 6x5, UPC: 637480055321, Case UPC: 637480059534. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 637480055321 | Day Break Chocolate Hazelnut Bar 6x5, UPC: 637480055321, Case UPC: 637480059534. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage |
| UPC | 637480059534 | Day Break Chocolate Hazelnut Bar 6x5, UPC: 637480055321, Case UPC: 637480059534. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage |
| best by | 10/23/2016 | Lot K52964, Best By 10/23/2016; Lot K53504, Best By 12/16/2016; Lot K53514, Best By 12/17/2016; Lot K53524, Best By 12/18/2016 |
| best by | 12/16/2016 | Lot K52964, Best By 10/23/2016; Lot K53504, Best By 12/16/2016; Lot K53514, Best By 12/17/2016; Lot K53524, Best By 12/18/2016 |
| best by | 12/17/2016 | K52964, Best By 10/23/2016; Lot K53504, Best By 12/16/2016; Lot K53514, Best By 12/17/2016; Lot K53524, Best By 12/18/2016 |
| best by | 12/18/2016 | K53504, Best By 12/16/2016; Lot K53514, Best By 12/17/2016; Lot K53524, Best By 12/18/2016 |
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-1716-2016
- Event ID
- 74340
- FDA status
- Terminated
- Initiated
- Jun 3, 2016
- Reported
- Jul 27, 2016
- Classified
- Jul 18, 2016
- Terminated
- Feb 13, 2017
- Quantity
- 17,033 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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