FDA recall record
Kwik Trip Cantaloupe, Item 930541. Net Wt 6 oz (170g). UPC 0 39779-00213 7. Produced & Distributed by Kwik Trip Inc., La Crosse WI
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 January 11, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Kwik Trip Cantaloupe, Item 930541. Net Wt 6 oz (170g). UPC 0 39779-00213 7. Produced & Distributed by Kwik Trip Inc., La Crosse WI
Reason
Potential Salmonella Contamination.
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.
Kwik Trip Cantaloupe, Item 930541. Net Wt 6 oz (170g). UPC 0 39779-00213 7. Produced & Distributed by Kwik Trip Inc., La Crosse WI
Code information listed by FDA
Sell By Date Range: 11/4/2023 - 12/3/2023
Distribution and firm information
Recalling firm listed by FDA: Kwik Trip, Inc.
Firm location listed by FDA: La Crosse, WI, United States
Distribution reported by FDA: IA, IL, MI, MN, SD, and WI
Product quantity listed by FDA: 77,013 units total
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.