FDA Recall United States TerminatedTerminated: January 11, 2024Historical recordClass I
Cut Fruit Express, Inc.
- Product
- Mixed Fruit Products that contain Cantaloupe, Honeydew, and…
- Published
- December 20, 2023
- Distribution
- IL, MN, & WI
Cut Fruit Express, Inc. Recall: Brie cheese has the potential to be contaminated with Listeria monocytogenes.
United States
TerminatedClass I
- Company
- Cut Fruit Express, Inc.
- Product
- Caribou Coffee Snack Fruit and Cheese Plate, item # 3818, Ne…
- Recall date
- October 5, 2022
- Terminated
- November 4, 2022
- Source
- FDA
Reason for recall
Brie cheese has the potential to be contaminated with Listeria monocytogenes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Caribou Coffee Snack Fruit and Cheese Plate, item # 3818, Net Wt 6.2 oz. (176g) 3 cheeses, red grapes, apples, rosemary crackers. Keep Refrigerated. Manufactured By: Cut Fruit Express, Inver Grove Heights, MN | Not published in this source record | 210 units | Use By: 9/30/2022, 10/2/2022, 10/4/2022, 10/7/2022 and 10/9/2022 |
Distribution
- MN
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0117-2023
- Event ID
- 90969
- Status
- Terminated
- Classification
- Class I
- Company
- Cut Fruit Express, Inc.
- Product description
- Caribou Coffee Snack Fruit and Cheese Plate, item # 3818, Net Wt 6.2 oz. (176g) 3 cheeses, red grapes, apples, rosemary crackers. Keep Refrigerated. Manufactured By: Cut Fruit Express, Inver Grove Heights, MN
- Quantity
- 210 units
- Reason
- Brie cheese has the potential to be contaminated with Listeria monocytogenes.
- Recall initiation date
- October 5, 2022
- Report date
- November 2, 2022
- Classification date
- Not published in this source record
- Termination date
- November 4, 2022
- Distribution pattern
- MN
- UPC, lot, and code information
- Use By: 9/30/2022, 10/2/2022, 10/4/2022, 10/7/2022 and 10/9/2022
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Cut Fruit Express, Inc.
Other recalls from Cut Fruit Express, Inc.
FDA Recall United States TerminatedTerminated: January 11, 2024Historical recordClass I
Cut Fruit Express, Inc.
- Product
- Mixed Fruit Products that contain Cantaloupe, Honeydew, Pine…
- Published
- December 20, 2023
- Distribution
- IL, MN, & WI
FDA Recall United States TerminatedTerminated: January 11, 2024Historical recordClass I
Cut Fruit Express, Inc.
- Product
- Mixed Fruit Products that contain Cantaloupe, Honeydew, Pine…
- Published
- December 20, 2023
- Distribution
- IL, MN, & 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 |
|---|---|
| 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.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
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.
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