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Lower risk Food recall · FDA · Published November 27, 2018

Kwik Trip Strawberry Parfait May Contain Almond and Cashew Tree Nuts

Kwik Trip recalls strawberry parfaits that may contain undeclared almond and cashew tree nuts. Consumers should check UPC 39779-18433 for affected products.

🇺🇸 FDA recall #F-0739-2019FoodKwik Trip ›
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Recalling firmKwik Trip, Inc.1626 Oak St · La Crosse, WI 54603-2308
✎ GovInfoNow plain-language explainer

Kwik Trip is recalling strawberry parfaits that may contain undeclared traces of almond and cashew tree nuts. People with allergies to these nuts should avoid the product to prevent allergic reactions. Read more at govinfonow.com/recall/18025-kwik-trip-strawberry-parfait-may-contain-almond-and-cashew-tree.

Source Summary by GovInfoNow · govinfonow.com/recall/18025-kwik-trip-strawberry-parfait-may-contain-almond-and-cashew-tree · Updated October 5, 2026 · FDA enforcement record: FDA #F-0739-2019

Cite this page

“Kwik Trip Strawberry Parfait May Contain Almond and Cashew Tree Nuts.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/18025-kwik-trip-strawberry-parfait-may-contain-almond-and-cashew-tree. Based on FDA recall #F-0739-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0739-2019%22&limit=1).

The FDA announced on 2018-11-27 that Kwik Trip, Inc. voluntarily recalled Kitchen Cravings Strawberry Parfait due to undeclared tree nuts. The product may contain traces of almond and cashew, posing an allergic reaction risk.

How to tell if you have it

  • Brand: Kwik Trip
  • Product: Kitchen Cravings Strawberry Parfait, Net Wt 8.25 oz (234g) Creamy Parfait Base, Strawberries with Sweetened Granola
  • UPC: 39779-18433
  • Sell by Date: on or before 12/6/2018
  • Distribution: IA, MN, WI
  • Units affected: 45,708

The hazard

Kitchen Cravings Strawberry and Mixed Berry Parfaits in an 8.25 oz. cup may contain undeclared traces of tree nuts, specifically almond and cashew.

Context

GovInfoNow's records show Kwik Trip, Inc. has had five other recalls since 2016-01-12. Recent brand recalls include a potential Salmonella contamination risk on 2023-11-27 and a potential Listeria or Salmonella contamination risk on 2018-10-15. Other recent recalls of similar products include Uncle Giuseppe's Milk Chocolate Bridge Mix (2026-04-20), Wilco Peanut Co Raw Shelled Peanuts Recall (2026-05-18), and George J Howe Sunflower Seed Tub Recall (2026-04-29).

How to tell if you have this one

Check for the UPC 39779-18433 on the product label. The product was sold in stores with the label 'Kitchen Cravings Strawberry Parfait, Net Wt 8.25 oz (234g)' between December 2018 and the sell-by date.

  • Brand
    Kwik Trip
  • Product
    Kitchen Cravings Strawberry Parfait, Net Wt 8.25 oz (234g) Creamy Parfait Base, Strawberries with Sweetened Granola
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    IA, MN, WI
Recall numberProduct, codes & lotsQuantity
F-0738-2019Kitchen 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; Sell by Date on or before 12/6/201850,452 units
F-0739-2019Kitchen 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; Sell by Date on or before 12/6/201845,708 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC 39779-18433 on the label to identify affected products.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “IA, MN, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Iowa, Minnesota, Wisconsin.

Recall timeline

FDA terminated this recall 24 days after the firm started it.

1. Firm started the recall: Nov 27, 201812. FDA classified it Class I: Dec 20, 201823. FDA terminated the recall: Dec 21, 201834. Published in FDA’s Enforcement Report: Dec 26, 201842018
  1. Firm started the recall
  2. FDA classified it Class I
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What should I do if I have the recalled product?

The recall does not require immediate action for people without nut allergies, but those with allergies should avoid the product.

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Where this comes from

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.

  • Official source: FDA Recall #F-0739-2019 (November 27, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0739-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA