Kwik Trip Mixed Fruit Tray, Item 930941. Net Wt 16 oz (1 lb.) 454g. UPC 0 39779-00248 4.
Kwik Trip, Inc. recalled this product and the FDA reported the enforcement action on 27 December 2023 as Class I. The recall was initiated by the firm. Potential Salmonella Contamination.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Kwik Trip Mixed Fruit Tray, Item 930941. Net Wt 16 oz (1 lb.) 454g. UPC 0 39779-00248 4. Produced & Distributed by Kwik Trip Inc., La Crosse WI
- UPC
- 039779002484
- Reason for recall
- Potential Salmonella Contamination.
- Recalling firm
- Kwik Trip, Inc.
- Firm location
- La Crosse, Wisconsin, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0621-2024
- Quantity
- 77,013 units total
- Distribution
- IA, IL, MI, MN, SD, and WI
- Initiated
- 27 November 2023
- Reported by FDA
- 27 December 2023
- Terminated
- 11 January 2024
- Firm notified by
- Press Release
- Product codes
- Sell By Date Range: 11/4/2023 - 12/3/2023
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 3 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 3 separate recalls, which almost every published figure does, overstates it by a factor of 3. All 3 of them are listed on this page.
- The recall ran for 6 weeks, from 27 November 2023 to termination on 11 January 2024. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 6 states, and the FDA published the enforcement report 4 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: Iowa, Illinois, Michigan, Minnesota, South Dakota, Wisconsin. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Salmonella
Salmonella is a bacterium that survives in low-moisture foods for months, which is why it appears in recalls of products that carry no water for it to grow in: nut butters, spices, flour and dry pet food.
A preventive controls plan covers Salmonella contamination under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(1)
- Process controls: the controls that apply a treatment, such as a validated kill step, at the point where it reduces the hazard to a safe level.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
- 21 CFR 117.165(a)(2)
- Product testing: testing as a verification activity, appropriate to the facility, the food and the nature of the preventive control.
Every product in this recall
The FDA opened 3 enforcement records for this one recall, one per product code. This page carries all of them; the 2 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2023-12-27 | 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 | Kwik Trip, Inc. | Potential Salmonella Contamination. | Class I |
| 2023-12-27 | Kwik Trip Cantaloupe, Item 930541. Net Wt 6 oz (170g). UPC 0 39779-00213 7. Produced & Distributed by Kwik Trip Inc., La Crosse WI | Kwik Trip, Inc. | Potential Salmonella Contamination. | Class I |
Other records from Kwik Trip, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 9 other records name this firm.
All 10 records for Kwik Trip, Inc.
All 2023 recalls · All FDA food recall data
21 CFR 117.135(c)(1) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. 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.
Early accessRecall 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.