Kwik Trip Strawberry Parfait Recall: Undeclared Peanuts or Almonds Risk
Kwik Trip recalls Kitchen Cravings Strawberry Parfaits that may contain undeclared peanuts or almonds. Consumers should check UPC 39779-18435 and sell-by dates for affected products.
Use caution until it’s fixed
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.
Contact the company
What happened, in plain English
Kwik Trip is recalling Kitchen Cravings Strawberry and Mixed Berry Parfaits due to potential undeclared traces of peanuts or almonds. This poses a risk for people with allergies, especially those allergic to peanuts or almonds. Read more at govinfonow.com/recall/23755-kwik-trip-strawberry-parfait-recall-undeclared-peanuts-or-almonds-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/23755-kwik-trip-strawberry-parfait-recall-undeclared-peanuts-or-almonds-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-2210-2016
Cite this page
“Kwik Trip Strawberry Parfait Recall: Undeclared Peanuts or Almonds Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23755-kwik-trip-strawberry-parfait-recall-undeclared-peanuts-or-almonds-risk. Based on FDA recall #F-2210-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2210-2016%22&limit=1).
Why it’s dangerous
The parfaits may contain undeclared traces of peanuts or almonds. This can trigger severe allergic reactions in people with allergies to these nuts, which can be life-threatening.
Who’s affected
People with peanut or almond allergies are most at risk from this recall. Anyone who purchased these parfaits from Kwik Trip stores is likely affected.
How to tell if you have this one
Check for the UPC 39779-18435 on the product label. The parfaits were sold with sell-by dates on or before July 21, 2016 for the initial recall and all dates in commerce for the expanded recall.
- Brand
Kwik Trip- Product
Kitchen Cravings Strawberry Parfait, Net Wt. 8.25 oz (234 g). UPC 39779-18435 Creamy Parfait Base, Strawberries with- Category
Food
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
Product distribution is limited to Kwik Trip, Inc. owned and operated retail stores located in Iowa, Minnesota and Wisconsin only.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-2210-2016 | Kitchen Cravings Strawberry Parfait, Net Wt. 8.25 oz (234 g). UPC 39779-18435 Creamy Parfait Base, Strawberries with Sweetened Granola. Keep Refrigerated.; All sell by dates on or before 7/21/16 for initial recall and All sell by dates in commerce for the expanded recall. | 10294 units from initial recall 7/21/16 & 1098 from expanded recall 7/20/16. |
| F-2211-2016 | Kitchen Cravings Mixed Berry Parfait, Net Wt. 8.25 oz (234 g). UPC 39779-18436 Creamy Parfait Base, Strawberries & Blueberries with Sweetened Granola. Keep Refrigerated.; All sell by dates on or before 7/21/16 for initial recall and All sell by dates in commerce for the expanded recall. | 18602 units from 7/21/16 recall & 11370 from expanded recall 7/29/16. |
What to do — step by step
Check Product Label
Look for the UPC 39779-18435 on the Kitchen Cravings Strawberry Parfait label.
Check Sell-By Date
The parfaits were sold with sell-by dates on or before July 21, 2016 for the initial recall and all dates in commerce for the expanded recall.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “Product distribution is limited to Kwik Trip, Inc. owned and operated retail stores located in Iowa, Minnesota and Wisconsin only.” 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 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-2210-2016 (July 21, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2210-2016 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.