FDA recall record

Cut Fruit Express Bruschetta Mix packaged under the following brands and sizes recall — FDA F-1106-2018

Bruschetta Dip and Bruschetta Mix are recalled because they contain undeclared Milk & Soy.

Class Iclassification
F-1106-2018official record ID
Apr 18, 2018report date

Recall record at a glance

Official recordF-1106-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmCut Fruit Express, Inc.
Report dateApr 18, 2018
Recall initiation dateApr 5, 2018
Quantity147 lbs.
LocationInver Grove Heights, MN, United States

Official 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.

Why the product was recalled

Bruschetta Dip and Bruschetta Mix are recalled because they contain undeclared Milk & Soy.

Distribution information

MN

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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