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FDA recall record

Day Break Cranberry Almond Bar 6x5, UPC: 637480055062, Case UPC: 637480059060. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage

Recall F-1710-2016Class ITerminatedJune 3, 2016

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of February 13, 2017. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Day Break Cranberry Almond Bar 6x5, UPC: 637480055062, Case UPC: 637480059060. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage

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.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • Day Break Cranberry Almond Bar 6x5, UPC: 637480055062, Case UPC: 637480059060. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage

Code information listed by FDA

Lot K52702, Best By 9/27/2016; Lot K52712, Best By 9/28/2016; Lot K52722, Best By 9/29/2016; Lot K52924, Best By 10/19/2016; Lot K52934, Best By 10/20/2016; Lot K52944, Best By 10/21/2016; Lot K53432, Best By 12/9/2016; Lot K53442, Best By 12/10/2016; Lot K53452, Best By 12/11/2016; Lot K60562, Best By 2/25/2017; Lot K60882, Best By 3/28/2017; Lot K60892, Best By 3/29/2017; Lot K60902, Best By 3/30/2017; Lot K61162, Best By 4/25/2017; Lot K61172, Best By 4/26/2017;

Distribution and firm information

Recalling firm listed by FDA: Atkins Nutritionals, Inc.

Firm location listed by FDA: Denver, CO, United States

Distribution reported by FDA: Nationwide. Canadian and foreign consignees. No VA/govt/military.

Product quantity listed by FDA: 112,531 cases

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.