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
Kwik Trip, Inc. Recall: Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic contaminating the ice.
United States
TerminatedClass II
- Company
- Kwik Trip, Inc.
- Product
- Ice Nuggets, 10 lb plastic bag, UPC 3977919140.
- Recall date
- January 12, 2016
- Terminated
- August 25, 2016
- Source
- FDA
Reason for recall
Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic contaminating the ice.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Ice Nuggets, 10 lb plastic bag, UPC 3977919140. | 3977919140 | Not published in this source record | Not published in this source record |
Distribution
- WI
- IA
- MN.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1835-2016
- Status
- Terminated
- Classification
- Class II
- Company
- Kwik Trip, Inc.
- Product description
- Ice Nuggets, 10 lb plastic bag, UPC 3977919140.
- Quantity
- Not published in this source record
- Reason
- Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic contaminating the ice.
- Recall initiation date
- January 12, 2016
- Report date
- August 3, 2016
- Classification date
- Not published in this source record
- Termination date
- August 25, 2016
- Distribution pattern
- WI, IA, MN.
- UPC, lot, and code information
- UPC 3977919140
- 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
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, 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 |
|---|---|
| Wisconsin | 1 |
| Iowa | 1 |
| Minnesota | 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 II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
