The FDA has published 10 food recall enforcement records naming Kwik Trip, Inc. between 2016 and 2023, covering 6 separate recall events. The firm is recorded in Wisconsin. Data last updated 2 September 2026.
Records of 29,386
10
Share of all recalls
0%
Class I of 10
8
Reported between
2016 to 2023
What these records are
Every record on this page was published by the FDA in the openFDA food enforcement database. 10 records cover 6 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.
8 of these records are Class I, 2 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.
What was recalled for
A single record can name more than one hazard, so these counts overlap.
Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.
Kwik Trip is recalling Kitchen Cravings Strawberry and Mixed Berry Parfaits because they may contain undeclared traces of peanuts. EXPANDED 7-29-2016 Kwik Trip has expanded their recall of Kitchen Craving Strawberry and Mixed Berry Parfaits because they may contain undeclared traces of peanuts or almonds.
Kwik Trip is recalling Kitchen Cravings Strawberry and Mixed Berry Parfaits because they may contain undeclared traces of peanuts. EXPANDED 7-29-2016 Kwik Trip has expanded their recall of Kitchen Craving Strawberry and Mixed Berry Parfaits because they may contain undeclared traces of peanuts or almonds.
Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic contaminating the ice.
Class II
Questions
How many FDA recalls has Kwik Trip, Inc. had?
The FDA has published 10 food recall enforcement records naming Kwik Trip, Inc. between 2016 and 2023. Those records cover 6 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?
Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.
A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.
