FDA Recall United States Terminated Historical recordClass I
Kwik Trip, Inc.
- Product
- Kitchen Cravings Mixed Berry Parfait, Net Wt 8.25 oz (234g)…
- Published
- December 26, 2018
- Distribution
- Multiple states
Kwik Trip, Inc. Recall: Kitchen Cravings Strawberry and Mixed Berry Parfaits in an 8.25 oz. cup may contain undeclared traces of tree nuts(specifically almond and cashew).
United States
TerminatedClass I
- Company
- Kwik Trip, Inc.
- Product
- Kitchen Cravings Strawberry Parfait, Net Wt 8.25 oz (234g)…
- Recall date
- November 27, 2018
- Terminated
- December 21, 2018
- Source
- FDA
Reason for recall
Kitchen Cravings Strawberry and Mixed Berry Parfaits in an 8.25 oz. cup may contain undeclared traces of tree nuts(specifically almond and cashew).
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | 39779-18433 | 45,708 units | Sell by Date on or before 12/6/2018 |
Distribution
- IA
- MN
- WI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0739-2019
- Event ID
- 81647
- Status
- Terminated
- Classification
- Class I
- Company
- Kwik Trip, Inc.
- Product description
- 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
- Quantity
- 45,708 units
- 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).
- Recall initiation date
- November 27, 2018
- Report date
- December 26, 2018
- Classification date
- Not published in this source record
- Termination date
- December 21, 2018
- Distribution pattern
- IA, MN, WI
- UPC, lot, and code information
- UPC 39779-18433; Sell by Date on or before 12/6/2018
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 81647 with 1 other product entry in Public Health Trace.
Responsible company: Kwik Trip, Inc.
Other recalls from Kwik Trip, Inc.
FDA Recall United States Terminated Historical recordClass I
Kwik Trip, Inc.
- Product
- Kwik Trip Mixed Fruit Tray, Item 930941. Net Wt 16 oz (1 lb…
- Published
- December 27, 2023
- Distribution
- IA, IL, MI, MN, SD, and WI
FDA Recall United States Terminated Historical recordClass I
Kwik Trip, Inc.
- Product
- Kwik Trip Mixed Fruit, Item 930847. Net Wt 6 oz (170g). UP…
- Published
- December 27, 2023
- Distribution
- IA, IL, MI, MN, SD, and WI
FDA Recall United States Terminated Historical recordClass I
Kwik Trip, Inc.
- Product
- Kwik Trip Cantaloupe, Item 930541. Net Wt 6 oz (170g). UPC…
- Published
- December 27, 2023
- Distribution
- IA, IL, MI, MN, SD, and WI
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Iowa | 1 |
| Minnesota | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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:
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.
