FDA recall record
Palmer's Candies Peppermint Bark A) NET WT 9 OZ (255 g) packaged in plastic clamshell containers, UPC Code 77232-17270; B) NET WT 10 OZ (283 g) packaged in paper bags, UPC 77232...
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 May 7, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Palmer's Candies Peppermint Bark A) NET WT 9 OZ (255 g) packaged in plastic clamshell containers, UPC Code 77232-17270; B) NET WT 10 OZ (283 g) packaged in paper bags, UPC 77232-23091; C) NET WT 8 OZ (226 g) packaged in paper boxes UPC 77232-12146; C) NET WT 9 OZ (255 g) packaged in plastic clamshell containers UPC 77232-16309; D) NET WT 9 OZ (255 g) packaged in paper boxes UPC 77232-16042; E) 10 lbs.
54 kg) packaged in cardboard boxes UPC 77232-10770
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
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.
Palmer's Candies Peppermint Bark A) NET WT 9 OZ (255 g) packaged in plastic clamshell containers, UPC Code 77232-17270; B) NET WT 10 OZ (283 g) packaged in paper bags, UPC 77232-23091; C) NET WT 8 OZ (226 g) packaged in paper boxes UPC 77232-12146; C) NET WT 9 OZ (255 g) packaged in plastic clamshell containers UPC 77232-16309; D) NET WT 9 OZ (255 g) packaged in paper boxes UPC 77232-16042; E) 10 lbs.
54 kg) packaged in cardboard boxes UPC 77232-10770
Code information listed by FDA
Exp 7/12/2017, 7/13/2017, 7/14/2017, 7/17/2017, 7/18/2017, 7/19/2017, 7/20/2017, 7/21/2017, 7/24/2017, 7/27/2017, 7/28/2017, 8/1/2017, 8/2/2017, 8/3/2017, 8/4/2017, 8/7/2017, 8/9/2017, 8/10/2017, 8/18/2017, 8/19/2017, 8/21/2017, 8/29/2017
Distribution and firm information
Recalling firm listed by FDA: Palmer and Company, dba Palmer Candy Co
Firm location listed by FDA: Sioux City, IA, United States
Distribution reported by FDA: Product distributed to grocery stores and grocery store distribution centers in AL, AR, AZ, CA, FL, GA, IA, IL, IN, KS, KY, LA, ME, MI, MN, MO, MS, NC, NE, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX, UT, VA, WA, WI, and WY
Product quantity listed by FDA: A) 3,675/16/9 OZ/clamshells/cases, B) 1,141/18/10 OZ/bags/cases, C) 7,538/24/8 OZ/boxes/cases D) 1/12/9 OZ/boxes/cases E) 1,021 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.