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CriticalFDAfda-F-2210-2016UNDECLARED ALLERGEN

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

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Units Affected
10,294
Recall Date
July 21, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2210-2016.

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.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2210-2016.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Kwik Trip, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2210-2016.

Kwik Trip, Inc.

FDA

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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Kwik Trip, Inc. Recall FAQ

Kwik Trip, Inc. is the subject of a bakery & grains safety report: Kitchen Cravings Strawberry Parfait, Net Wt. 8.25 oz (234 g). UPC 39779-18435 Creamy Parfait Base, Strawberries with Sweetened Granola..... The notice was published on July 21, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 10,294 units are potentially affected.