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

Triple Chocolate 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.

ProductTriple Chocolate Bar 6x5, UPC: 637480035408, Case UPC: 637480034005. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
UPC637480034005, 637480035408

FDA code information

Lot K61182, Best By 4/27/2017

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Full FDA record and distribution details

Original product description

Triple Chocolate Bar 6x5, UPC: 637480035408, Case UPC: 637480034005. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage

Extracted codes and context

TypeCode / valueContext
UPC637480034005Triple Chocolate Bar 6x5, UPC: 637480035408, Case UPC: 637480034005. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
UPC637480035408Triple Chocolate Bar 6x5, UPC: 637480035408, Case UPC: 637480034005. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
best by4/27/2017Lot K61182, Best By 4/27/2017

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-1719-2016
Event ID
74340
FDA status
Terminated
Initiated
Jun 3, 2016
Reported
Jul 27, 2016
Classified
Jul 18, 2016
Terminated
Feb 13, 2017
Quantity
784 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-1719-2016

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

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