Food recall
Kwik Trip, Inc. recall: Kitchen Cravings Mixed Berry Parfait
Kwik Trip, Inc., of La Crosse, WI, recalled Kitchen Cravings Mixed Berry Parfait and 1 other product. The FDA's reason: “Kitchen Cravings Strawberry and Mixed Berry Parfaits in an 8.25 oz. cup may contain undeclared traces of tree nuts(specifically almond and cashew).” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on November 27, 2018, and the FDA first listed it in its Enforcement Report of December 26, 2018. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class I
It could cause serious harm or death
Why
Allergen not on the label
Status
Terminated
Closed December 21, 2018
The recall
- Company
- Kwik Trip, Inc. (La Crosse, WI)
- Reason, in FDA's words
- “Kitchen Cravings Strawberry and Mixed Berry Parfaits in an 8.25 oz. cup may contain undeclared traces of tree nuts(specifically almond and cashew).”
- Where it was sold
- IA, MN, WI
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 81647
The 2 products recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-0738-2019 Class I
Kitchen Cravings Mixed Berry Parfait, Net Wt 8.25 oz (234g) Creamy Parfait Base, Strawberries & Blueberries with Sweetened Granola. Keep Refrigerated. UPC 39779-18436. Produced and Distributed by Kwik Trip, Inc., La Crosse, WI 54603
Codes: Sell by Date on or before 12/6/2018
Quantity: 50,452 units
-
F-0739-2019 Class I
Kitchen Cravings Strawberry Parfait, Net Wt 8.25 oz (234g) Creamy Parfait Base, Strawberries with Sweetened Granola. Keep Refrigerated. UPC 39779-18433. Produced and Distributed by Kwik Trip, Inc., La Crosse, WI 54603
Codes: Sell by Date on or before 12/6/2018
Quantity: 45,708 units
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of December 26, 2018.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.