Recalls / Class I
Class IF-0620-2024
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
Kwik Trip Mixed Fruit, Item 930847. Net Wt 6 oz (170g). UPC 0 39779-00240 3. Produced & Distributed by Kwik Trip Inc., La Crosse WI
- Type
- Food
- Affected lot / code info
- Sell By Date Range: 11/4/2023 - 12/3/2023
- Quantity
- 77,013 units total
Why it was recalled
Potential Salmonella Contamination.
Recalling firm
- Firm
- Kwik Trip, Inc.
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- 1626 Oak St, N/A, La Crosse, Wisconsin 54603-2308
Distribution
- Distribution pattern
- IA, IL, MI, MN, SD, and WI
Timeline
- Recall initiated
- 2023-11-27
- FDA classified
- 2023-12-16
- Posted by FDA
- 2023-12-27
- Terminated
- 2024-01-11
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0620-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings.