Check the Batch
Class ITerminated in FDA datasetRecall initiated Jun 3, 2016

Cinnamon Bun 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…

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.

Check your package

Compare the exact product and package details with the label you have.

ProductCinnamon Bun Crisp Bar 6x5, UPC: 637480059251, Case UPC: 637480005906. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
UPC637480005906, 637480059251

FDA code information

Lot K53484, Best By 12/14/2016

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Full FDA record and distribution details

Original product description

Cinnamon Bun Crisp Bar 6x5, UPC: 637480059251, Case UPC: 637480005906. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage

Extracted codes and context

TypeCode / valueContext
UPC637480005906Cinnamon Bun Crisp Bar 6x5, UPC: 637480059251, Case UPC: 637480005906. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
UPC637480059251Cinnamon Bun Crisp Bar 6x5, UPC: 637480059251, Case UPC: 637480005906. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
best by12/14/2016Lot K53484, Best By 12/14/2016

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-1711-2016
Event ID
74340
FDA status
Terminated
Initiated
Jun 3, 2016
Reported
Jul 27, 2016
Classified
Jul 18, 2016
Terminated
Feb 13, 2017
Quantity
9,782 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-1711-2016

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

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