← FDA ENFORCEMENT
F-0619-2024Class I

Kwik Trip, Inc.

Recalling firm
Kwik Trip, Inc.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2023-12-27
Distribution
IA, IL, MI, MN, SD, and WI
Firm state
WI
Product quantity
77,013 units total
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential Salmonella Contamination.

Product description

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 / lot info

Sell By Date Range: 11/4/2023 - 12/3/2023

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.