Kwik Trip, Inc. Recall: 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.

🇺🇸 United States

1. July 21, 2016 - Recall initiated
2. September 21, 2016 - Reported by source
3. October 11, 2016 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2210-2016

Status

Terminated

Classification

Class I

Company

Kwik Trip, Inc.

Product description

Kitchen Cravings Strawberry Parfait, Net Wt. 8.25 oz (234 g). UPC 39779-18435 Creamy Parfait Base, Strawberries with Sweetened Granola. Keep Refrigerated.

Quantity

Not published in this source record

Reason

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.

Recall initiation date

July 21, 2016

Report date

September 21, 2016

Classification date

Not published in this source record

Termination date

October 11, 2016

Distribution pattern

Product distribution is limited to Kwik Trip, Inc. owned and operated retail stores located in Iowa, Minnesota and Wisconsin only.

UPC, lot, and code information

UPC 39779-18435

Voluntary or mandated

Not published in this source record

Initial notification method

Not published in this source record

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Kwik Trip, Inc.

Other recalls from Kwik Trip, Inc.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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