Kwik Trip recalls mixed fruit trays (item 930941) produced between November 4 and December 3, 2023, due to potential Salmonella contamination. Consumers should check product details and follow official recall steps.
Potential Salmonella Contamination.
Kwik Trip is recalling mixed fruit trays (item 930941) that were produced between November 4 and December 3, 2023. These products may contain Salmonella, which can cause foodborne illness. Consumers should stop using the product if they have it and follow the recall instructions.
Salmonella is a bacteria that can cause food poisoning, leading to symptoms like diarrhea, fever, and stomach cramps. The contamination in these fruit trays could occur during production or handling, posing a risk if the product is consumed.
Anyone who purchased the Kwik Trip Mixed Fruit Tray (item 930941) between November 4 and December 3, 2023. People with compromised immune systems are at higher risk from Salmonella.
Check for the product name 'Kwik Trip Mixed Fruit Tray', item number 930941, and a sell-by date between November 4 and December 3, 2023. The UPC code is 0 39779-00248 4.
Look for the item number 930941 and sell-by date between November 4 and December 3, 2023 on the product label.
The recall states there is potential Salmonella contamination, so it is not safe to eat. Consumers should stop using the product and follow the recall instructions.
Check for the product name 'Kwik Trip Mixed Fruit Tray', item number 930941, and a sell-by date between November 4 and December 3, 2023.
The recall does not specify a remedy, so consumers should check with Kwik Trip for further instructions or contact the FDA for assistance.
We’ve drafted a message you can send Kwik Trip to request your refund or repair — edit it as you like.
Subject: Recall F-0621-2024 — Kwik Trip Kwik Trip Hello, I own a Kwik Trip that is covered by recall F-0621-2024 from Kwik Trip. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
