FDA Recall United States Terminated Historical 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: Bruschetta Dip and Bruschetta Mix are recalled because they contain undeclared Milk & Soy.
United States
TerminatedClass I
- Company
- Cut Fruit Express, Inc.
- Product
- Bruschetta Mix packaged under the following brands and sizes…
- Recall date
- April 5, 2018
- Terminated
- June 27, 2019
- Source
- FDA
Reason for recall
Bruschetta Dip and Bruschetta Mix are recalled because they contain undeclared Milk & Soy.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Bruschetta Mix packaged under the following brands and sizes: 1. Tastebuds, Net Wt. 12 oz. (340g), UPC 38232-37403. Shipping case: H. Brooks, 37403, Net wt. 12 oz. (340g), K*319, Keep Refrigerated, 6 units per case, Distributed by H. Brooks & Co Mpls. MN 55112. 2. Quick & Easy Fresh Cut, Net Wt. 12 oz. (340g) UPC 38232-37403, shipping case: Supervalu, 38591, 6/12 oz., Net Wt 5.30 lbs., SV*069, Keep Refrigerated, 6 units per case Distributed by Supervalu, Eden Prairie, MN 55344. 3. H. Brooks, 38914, Bruschetta 5#, K*195, Keep Refrigerated, 1 unit per case, Distributed by H. Brooks & Co Mpls, MN 55112. 4. Reinhart, 82826, Brushetta Mix, 5#, Manufactured by Cut Fruit Express Mpls. MN 55076 5. Upper Lakes Foods, 143900, Bruschetta Mix, 5#, UPC 00001-43900, Manufactured by Cut Fruit Express Mpls. MN 55076. | 38232-37403 | 147 lbs. | Use by Dates: 4/5/2018 - 4/12/2018 |
Distribution
- MN
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1106-2018
- Event ID
- 79771
- Status
- Terminated
- Classification
- Class I
- Company
- Cut Fruit Express, Inc.
- Product description
- Bruschetta Mix packaged under the following brands and sizes: 1. Tastebuds, Net Wt. 12 oz. (340g), UPC 38232-37403. Shipping case: H. Brooks, 37403, Net wt. 12 oz. (340g), K*319, Keep Refrigerated, 6 units per case, Distributed by H. Brooks & Co Mpls. MN 55112. 2. Quick & Easy Fresh Cut, Net Wt. 12 oz. (340g) UPC 38232-37403, shipping case: Supervalu, 38591, 6/12 oz., Net Wt 5.30 lbs., SV*069, Keep Refrigerated, 6 units per case Distributed by Supervalu, Eden Prairie, MN 55344. 3. H. Brooks, 38914, Bruschetta 5#, K*195, Keep Refrigerated, 1 unit per case, Distributed by H. Brooks & Co Mpls, MN 55112. 4. Reinhart, 82826, Brushetta Mix, 5#, Manufactured by Cut Fruit Express Mpls. MN 55076 5. Upper Lakes Foods, 143900, Bruschetta Mix, 5#, UPC 00001-43900, Manufactured by Cut Fruit Express Mpls. MN 55076.
- Quantity
- 147 lbs.
- Reason
- Bruschetta Dip and Bruschetta Mix are recalled because they contain undeclared Milk & Soy.
- Recall initiation date
- April 5, 2018
- Report date
- April 18, 2018
- Classification date
- Not published in this source record
- Termination date
- June 27, 2019
- Distribution pattern
- MN
- UPC, lot, and code information
- UPC 38232-37403; Use by Dates: 4/5/2018 - 4/12/2018
- 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
Responsible company: Cut Fruit Express, Inc.
Other recalls from Cut Fruit Express, Inc.
FDA Recall United States Terminated Historical 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 Terminated Historical 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.
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.
